The Online Seminar shows the Possibilities of the use of Desktop-Sharing Software. The Online-Seminar is free of charge an will contain the following topic.
How to Setup the Software.
Cost of the Software
Usage in the Sales and Marketing area.
The Webinar will held on request\, the duration is approx. 30 Minutes
Further Information to the Online-Seminar
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120201T111100Z DTEND;VALUE=DATE-TIME:20120201T111100Z UID:http://www.webinarcentral.net/content/2012-perspectives-solar-energy-markets-technologies-projects-and-developments-1 URL;VALUE=URI:http://www.webinarcentral.net/content/2012-perspectives-solar-energy-markets-technologies-projects-and-developments-1 SUMMARY:2012 Perspectives on Solar Energy\: markets\, technologies\, projects and developments DESCRIPTION:Solar Energy is looking to be the bright spot in renewable energy\, with huge potential and opportunities.
Various studies\, amongst others by The World Bank\, were conducted to understand the “ground level” barriers that the developers are facing.
In general 5 parameters (Policy and Regulations\, Technology\, Solar Radiation Data\, Infrastructure and Financing) cover the development cycle of solar power projects.
Solar Energy is looking to be the bright spot in renewable energy\, with huge potential and opportunities.
Various studies\, amongst others by The World Bank\, were conducted to understand the “ground level” barriers that the developers are facing.
In general 5 parameters (Policy and Regulations\, Technology\, Solar Radiation Data\, Infrastructure and Financing) cover the development cycle of solar power projects.
Solar Energy is looking to be the bright spot in renewable energy\, with huge potential and opportunities.
Various studies\, amongst others by The World Bank\, were conducted to understand the “ground level” barriers that the developers are facing.
In general 5 parameters (Policy and Regulations\, Technology\, Solar Radiation Data\, Infrastructure and Financing) cover the development cycle of solar power projects.
This webinar will cover the various methods used to determine residual moisture in products ranging from bulk powders\, to sterile freeze-died products in vials\, to foods.
Monitoring and controlling residual moisture in powders\, lyophilized solids\, foods\, etc can be a critical factor in achieving and maintaining quality products throughout their expected shelf life. Improper levels of moisture in products can result in poor powder flow properties\, spoilage\, polymorph changes\, changes in compaction properties\, microorganism growth promotion\, higher degradation kinetics\, and in the case of freeze-dried products\, loss of physical structure and changes in reconstitution properties.
There are several methods typically employed to determine residual moisture\, and the choice of method will be based on the sample tested\, the level of residual moisture present\, and the accuracy and precision required for testing. Additionally\, many of these methods require a skill and knowledge in preparing and testing the samples if accurate results are to be achieved. In fact\, in many cases\, samples containing very low residual moisture\, as in the case with freeze-dried products\, accurate results for residual moisture are not achieved simply due to improper sample preparation and handling.
Additionally\, inaccurate and or imprecise results will be obtained if the correct method for testing residual moisture is not chosen. In addition to covering the various techniques employed for residual moisture testing\, this seminar will pay particular attention to choosing the correct technique for a specific application\, specific details of sample preparation\, sample handling\, and data analysis\, all of which can affect the final result.
In addition\, a high throughput\, non-destructive technique will be discussed\, which can be used\, if applied correctly\, for very rapid and accurate testing with 100% sample recovery.
Areas Covered in the Session\:
Thermal properties of formulated products
How and where residual moisture is trapped in products
Effects of residual moisture on dried products
Gravimetric methods for residual moisture testing
Near infrared spectroscopy method for residual moisture testing
Volumetric Karl Fischer titration
Coulometric Kark Fischer titration
Specialized methods of residual moisture testing
Proper handling techniques for external extraction in sealed vials
Learning objectives\:
Choosing the correct residual moisture test for your applications
Understanding the advantages and disadvantages of the different techniques covered
Understanding (via a step by step method) the proper technique for conducting a coulometric Karl Fischer external extraction (including equations)
Who Will Benefit\:
Quality Control Scientists
Development Scientists
Production Management
Quality Assurance
Price List\:
Live \: $245.00
Corporate live \: $995.00
Recorded \: $295.00
webinars@globalcompliancepanel.com
http\://www.globalcompliancepanel.com
Phone\: 800-447-9407
Fax\: 302-288-6884
1000 N West Street | Suite 1200 | Wilmington | DE | Zip 19801 | USA
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120201T180000Z DTEND;VALUE=DATE-TIME:20120201T180000Z UID:http://www.webinarcentral.net/content/efficient-computer-system-validation-10-easy-steps-webinar-globalcompliancepanel-0 URL;VALUE=URI:http://www.webinarcentral.net/content/efficient-computer-system-validation-10-easy-steps-webinar-globalcompliancepanel-0 SUMMARY:Efficient Computer System Validation - 10 Easy Steps - Webinar By GlobalCompliancePanel DESCRIPTION:This webinar details all of the templates used to create validation documentation\, usually saving two-thirds of the time and costs.
The 10-step risk-based approach to COTS software validation minimized documentation and ensures efficient implementation of new and upgraded computer systems. This experience will prepare you to perform a validation project.
Areas Covered in the Session\:
Learn which documents the FDA expects to audit.
How to use the risk-based validation approach to lower costs.
How to link requirements\, specifications\, risk management\, and testing.
Document a computer system validation project using easy to understand fill-in-the-blank templates.
Based on\: \\"Risk-Based Software Validation – Ten Easy Steps\\" (Davis Horwood International and PDA - www.pda.org\, 2006).
Step-by-step instructions for performing and documenting a risk assessment\, and how to use the results to reduce validation documentation.
Reduce testing by writing test cases that trace to elements of risk management.
Who Will Benefit\:
IT
QA
QC
Laboratory staff
Managers
GMP\, GCP\, GLP professionals
Price List\:
Live \: $245.00
Corporate live \: $995.00
Recorded \: $295.00
webinars@globalcompliancepanel.com
http\://www.globalcompliancepanel.com
Phone\: 800-447-9407
Fax\: 302-288-6884
1000 N West Street | Suite 1200 | Wilmington | DE | Zip 19801 | USA
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120201T160000Z DTEND;VALUE=DATE-TIME:20120201T160000Z UID:http://www.webinarcentral.net/content/performance-management-magic-face-face-conversation-webinar-trainhr URL;VALUE=URI:http://www.webinarcentral.net/content/performance-management-magic-face-face-conversation-webinar-trainhr SUMMARY:Performance Management\: The Magic of the Face-to-Face Conversation - Webinar By TrainHR DESCRIPTION:Overview \: It is often called the \\"most dreaded management task\\". It's the performance management conversation. How do you turn poor performance around without soft peddling the difficult stuff or being hypercritical and risking a defensive reaction?
In this program\, Judi Clements prepares your managers &\; supervisors for this difficult\, yet very important\, job. Without a successful performance management process\, organizations can fall into the trap of \\"carrying\\" poor performers &\; tacitly endorsing substandard work. Judi shows your leaders how to utilize your organization's performance management system and use behavioral\, not attitudinal language to ensure legal compliance and optimal employee development. Judi turns the \\"most dreaded management task\\" into a positive experience for all.
Why you should attend\: To develop the skills to prepare\, deliver\, and follow-up performance management interventions with low performing employees.
Areas Covered in the Session\:
Develop Rapport with Employees
Set a Self-motivating Workplace Climate
Monitor Employee Performance
Provide Effective Feedback
Coach Employees to Perform at Higher Levels
Prepare for Performance Management Meetings
Encourage Employees to Self-appraise
Encourage Employees to Identify Areas for Improvement and Set Appropriate Goals
Anticipate &\; Manage Employee Defensiveness\, Anger\, or Other Emotions
Follow-up Performance Management Interventions
Who Will Benefit\:
Managers
Supervisors
Leaders
Human Resource Professionals
Shift Leaders
Oppositional Defiant Disorder doesn’t have to be complicated! This web course provides mental health professionals with a three-step approach to treating the signs and symptoms of ODD and co-occurring disorders in children and teens\,
ages 4-14.
Full Description\:
Confronting Defiance
According to the AACAP\, evidence suggests that between 1 and 16% of children and adolescents have Oppositional Defiant Disorder (ODD). Challenged by basic rules of society\, this disorder causes a struggle between the parent and child and
ultimately the therapist and child. Tantrums\, arguing\, defiance\, blaming\, and anger when left untreated may disrupt classrooms\, strain families\, and lead to a risk of juvenile delinquency. Conflict may also go on to affect the
behavioral\, academic\, and social success of the child.
This webinar discusses ODD\, similar disorders\, and the effect on young children and teens. Using a three-step approach to intervention called SimpleThree\, mental health professionals will learn how to treat ODD symptoms in children and
adolescents as well as educate parents to reinforce good behavior to maintain success.
Course Includes\:
Live Q&\;A
Presentation Handout
Post session recording access
CE Credit
What You Will Learn\:
Identify Oppositional Defiant Disorder\, children at risk\, and differentiate from similar childhood diagnoses by etiology and behavior
Apply a three-step\, evidence-based approach to intervention called SimpleThree with defiant children ages 4-14
Incorporate a behavioral modification system using clear\, measurable rules to encourage good behavior and structure
Learn how to strategically follow up with families to reinforce effective parenting skills and maintain success and support with easy-to-access resources
Your Presenter\:
WARD HALVERSON\, LCSW-R\, M.Ed.\, is a licensed clinical social worker and educator with over 12 years of experience as well as a former school teacher\, army veteran and medical officer\, and father. He received a master’s degree in Social
Work from Syracuse University and a master’s degree in education from The College of Saint Rose. Mr. Halverson currently runs an outpatient mental health private practice where he specializes in the treatment of child and family
defiance\, anxiety\, and trauma\, and has developed the SimpleThree system to approach these issues with his clients as well as other mental health professionals.
Disclaimer\:
This event qualifies for one CE credit. Only registered attendees will have access to CE. A Cross Country Education web account is required to attend. There is no charge for a CCE web account. It is recommended that you join the meeting
15 to 20 minutes early. Speaker phone sound quality is poor and it is recommended that they not be used to listen to the event.
Technical requirements\:
To view this webinar you will need to download the WebEx Application. You will be prompted to download it when you first enter the site. To save time\, you can setup prior to the meeting by following this link\:
https\://apidemoeu.webex.com/apidemoeu/meetingcenter/mcsetup.php
Who Should Attend\:
Social Workers\, Psychiatric Nurses\, School Nurses\, Psychiatric Nurse Practitioners\, Licensed Professional Counselors\, Marriage and Family Therapists\, Psychologists\, Educators\, School Social Workers\, School Administrators\, Foster Care
Professionals\, Parents\, Clergy
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120201T133000Z DTEND;VALUE=DATE-TIME:20120201T133000Z UID:http://www.webinarcentral.net/content/upcoming-free-webinar-storage-testing-overview URL;VALUE=URI:http://www.webinarcentral.net/content/upcoming-free-webinar-storage-testing-overview SUMMARY:Upcoming Free Webinar on \\"Storage Testing - Overview\\" DESCRIPTION:Storage is a premium sector of our software industry. It is bit crucial to handle but it is one of the most demanding area. Special skill-sets are required to work on storage domain. There are comparatively less people who are willing to work in this area. This webinar will mainly put light on the overview of the storage testing activity.
Agenda\:
- Concept of storage
- Storage management techniques\: SAN\, NAS
- Why to test storage?
- Storage testing types
- Skill-sets required for storage testing
- FAQs
Free Registration\: https\://www1.gotomeeting.com/register/413558177
Read More\: http\://www.vyomlabs.com/resources/webinars/overview-storage-testing/
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120202T130000Z DTEND;VALUE=DATE-TIME:20120202T190000Z UID:http://www.webinarcentral.net/content/full-day-virtual-seminar-understanding-and-effectively-controlling-biofilm-pharmaceutical-w-0 URL;VALUE=URI:http://www.webinarcentral.net/content/full-day-virtual-seminar-understanding-and-effectively-controlling-biofilm-pharmaceutical-w-0 SUMMARY:Full Day Virtual Seminar\: Understanding and Effectively Controlling Biofilm in Pharmaceutical Water Systems DESCRIPTION:This 6-hr training will focus on important microbial issues with pharmaceutical water systems and provide proven solutions for microbial control. Attendees will learn effective sanitation and validation approaches to successfully control biofilm in water systems.
Why Should You Attend\:
This interactive one-day course provides a thorough understanding of what makes water systems have microbial problems with proven solutions for microbial control. It also details how to validate that control by determining the operations and processes that logically must be evaluated in pharmaceutical water and steam systems during the validation exercise in a manner that will please FDA.
Finally\, and perhaps most importantly\, attendees will learn how to institute simple sampling\, monitoring and microbial control levels that will dramatically reduce microbial excursions and facilitate having successful and accurate root cause investigation outcomes.
In short\, if your job brings you in contact with any aspect of water system design\, maintenance\, trend monitoring\, sampling\, testing\, sanitization\, validation\, responses to microbial excursions\, root cause investigations\, or regulatory interactions\, you cannot afford to miss this invaluable training as well as the tips\, tricks\, and kernels of wisdom that this all-day webinar will give you.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120202T170000Z DTEND;VALUE=DATE-TIME:20120202T170000Z UID:http://www.webinarcentral.net/content/wso2-business-activity-monitor-bam-20-new-beginning URL;VALUE=URI:http://www.webinarcentral.net/content/wso2-business-activity-monitor-bam-20-new-beginning SUMMARY:WSO2 Business Activity Monitor (BAM) 2.0 - a new beginning DESCRIPTION:Monitoring business activities in a service oriented architecture (SOA) translates into monitoring relevant web services. This means that capturing messages and statistics from servers deployed in the SOA deployment should be trivial to monitor and gain an insight into what happens in an organization.
Though this is the case\, a monitoring solution needs to wary of other factors that get involved in serious monitoring use cases\:
Customization - Different groups within an organization will have different requirements\, thereby requiring to define different key performance indicators. (KPIs).
Robustness - Monitoring should have virtually zero impact on the servers which are monitored\, and should be able to handle any failure gracefully.
Performance - Colossal loads passing through SOA deployments is quite common\, and the monitoring solution should be able to handle same.
Scalability - It should be scalable in multiple senses\, by message load\, by data volume\, by processing volume etc.
WSO2 BAM 2.0 is a complete re-write of the BAM 1.x version\, based on lessons learnt in order to suit the requirements stated above. This session will discuss how we address these requirements based on NoSQL data storage\, super fast data transfer rates\, configuration based analytics and WYSIWIG UI development tools.
Tharindu\, Product Manager of BAM and Senior Software Engineer\, has been involved in Web Service technologies for 3 years. He has practical experience working with projects like Apache Cassandra\, Apache Hadoop\, Apache Thrift and various other open source projects. He has been involved in many development projects in various countries in Europe\, Asia and the Americas.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120202T150000Z DTEND;VALUE=DATE-TIME:20120202T150000Z UID:http://www.webinarcentral.net/content/oracle-clinical-and-remote-data-capture-implementation-standards-and-best-practices URL;VALUE=URI:http://www.webinarcentral.net/content/oracle-clinical-and-remote-data-capture-implementation-standards-and-best-practices SUMMARY:Oracle Clinical and Remote Data Capture Implementation Standards and Best Practices DESCRIPTION:As your organization implements or upgrades to a newer version of Oracle Clinical (OC) and Remote Data Capture (RDC)\, there are many considerations to take into account. Educating yourself on best practices and learning from past mistakes are all are critical components for a successful installation of your clinical data management and EDC systems\, and the establishment of good standards.
Join BioPharm Systems' Lori Venable\, principal consultant\, clinical data management\, for this one-hour session that will examine various OC and RDC implementation and usage best practices that all sponsors and CROs should consider to greatly increase the usability of the applications\, as well as boost user productivity.
This webinar will cover best practices in the following areas\:
• Training
• User roles and functions
• SOPs and Work Instructions
• Implementation\, upgrade and usage standards
• … and much more!
Thursday\, February 2\, 2012 @\:
7\:00 a.m. Pacific Time
8\:00 a.m. Mountain Time
9\:00 a.m. Central Time
10\:00 a.m. Eastern Time
15\:00 UK Time
16\:00 Central European Time
In this CLIA inspection webinar understand how to get your lab ready for inspection\, what the inspectors will look for and how to do inspection follow up and response.
Why Should You Attend\:
All clinical laboratories (except waived laboratories) are inspected every two years by the federal government\, a state agency\, or a private accreditation organization. The CLIA inspection process can be a daunting experience. Compliance with the CLIA regulations is essential and is required to keep the ability to test specimens.
Although the inspection can be some what subjective\, there are many elements of the process that are standard among all inspectors. Understanding the inspection process and knowing what is expected can take the stress out of hearing “Your inspection is tomorrow”.
Is your lab ready for an on-site inspection? Do you have your lab in order? Do you know what to inspect when they arrive? This webinar will address all these questions and more. Preparation is the cornerstone of the process and makes all the difference between success and failure. Let us help your lab be as ready as possible for inspection and to take the mystery out of the inspection process.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120202T180000Z DTEND;VALUE=DATE-TIME:20120202T180000Z UID:http://www.webinarcentral.net/content/risk-analysis-portfolio-drug-development-programs-webinar-globalcompliancepanel URL;VALUE=URI:http://www.webinarcentral.net/content/risk-analysis-portfolio-drug-development-programs-webinar-globalcompliancepanel SUMMARY:Risk Analysis for Portfolio of Drug Development Programs - Webinar By GlobalCompliancePanel DESCRIPTION:Building in strategic risk scenarios into portfolio planning can buffer the organization against the unexpected. Examples might be clinical trial failure\, shifts in the marketplace or insufficient resource capacity. This webinar covers various portfolio planning tools and techniques with a focus on strategic risk management.
Key Questions to Be Addressed\:
How to align strategic goals and available resources?
What strategic risks company should be prepared for?
How to incorporate risk in portfolio planning?
What tools could be used for portfolio planning to analyze portfolio selection\, capacity planning and risk management?
How to simulate risk mitigation strategies?
Why you should attend\: Neglecting risk assessment in portfolio planning could ruin company strategy. Major source of uncertainty is outcome of clinical trial. Another source is marketing predictions. Therefore\, portfolio planning based on averages\, could mislead executive management. Some companies use simplistic risk assessment portfolio models. They do not take into account interdependencies between drug development projects. Unfortunately\, those models are inaccurate\, and generate misleading results.
Areas Covered in the Session\:
What strategic risks company should be prepared for?
How to incorporate risk in portfolio planning?
What tools could be used for portfolio planning to analyze portfolio selection\, capacity planning and risk management?
How to simulate risk mitigation strategies?
Who Will Benefit\:
Portfolio planning\, VP\, Director\, manager
Financial analysts\, Directors\, VPs\, managers
Clinical Operations\, VP\, Director\, planner\, manager
Business Development\, VP\, Director\, analyst\, manager
Discovery portfolio\, VP\, Director\, manager
Manufacturing\, VP\, Director\, manager
Marketing\, VP\, Director Manager
Price List\:
Live \: $245.00
Corporate live \: $995.00
Recorded \: $295.00
webinars@globalcompliancepanel.com
http\://www.globalcompliancepanel.com
Phone\: 800-447-9407
Fax\: 302-288-6884
1000 N West Street | Suite 1200 | Wilmington | DE | Zip 19801 | USA
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120202T170000Z DTEND;VALUE=DATE-TIME:20120202T170000Z UID:http://www.webinarcentral.net/content/new-slant-childhood-developmental-disorders-ocd-tics-pandas-nonverbal-learning-disability-an URL;VALUE=URI:http://www.webinarcentral.net/content/new-slant-childhood-developmental-disorders-ocd-tics-pandas-nonverbal-learning-disability-an SUMMARY:A New Slant on Childhood Developmental Disorders\: OCD\, Tics\, PANDAS\, Nonverbal Learning Disability\, and Dysgraphia DESCRIPTION:A fresh\, innovative approach to Childhood Developmental Disorders
Full Description\:
During this webinar a selection of childhood developmental disorders will be depicted and treatment strategies including medication management will be outlined. Obsessive-Compulsive Disorder and Tic Disorder\, part of a triad of disorders characterized by malfunction of the fronto-striatal circuitry\, will be discussed. PANDAS\, a newly described disorder that can mimic a triad disorder with its symptoms overlapping those of OCD and Tics\, will be introduced and examined. Symptoms of Nonverbal Learning Disabilities will be reviewed and compared with the other disorders. Finally\, brand new\, innovative research on Dysgraphia will be introduced with new methods to help children with handwriting.
Course Includes\:
Live Q&\;A
Presentation Handout
Post session recording access
CE Credit
What You Will Learn\:
Describe the DSM IV criteria for OCD and explain why it is part of the Triad
List the DSM IV criteria for Tic Disorder and explain its role in the Triad
Define NVLD and contrast it with Asperger’s Disorder
Discuss the neurodevelopment of the right hemisphere
Outline the symptoms of Dysgraphia
Your Presenter\:
ANITA REMIG\, Ed.D.\, F.P.P.R.\, F.S.M.I.\, is a practicing clinical psychologist\, certified school psychologist\, and consultant with over 25 years of experience specializing in learning styles\, brain-based research\, and learning problem interventions. Dr. Remig is a member of the American Psychological Association. She is a “Fellow of the Prescribing Psychologist Register” (F.P.P.R.) and a “Fellow in Serious Mental Illness” (F.S.M.I.) from the Prescribing Psychologist Register. Dr. Remig also recently passed the ICCP National Examination for Psychologists in Psychopharmacology and has been awarded a certification as a Medical Psychologist from the Academy of Medical Psychology.
Disclaimer\:
This event qualifies for one CE credit. Only registered attendees will have access to CE. A Cross Country Education web account is required to attend. There is no charge for a CCE web account. It is recommended that you join the meeting 15 to 20 minutes early. Speaker phone sound quality is poor and it is recommended that they not be used to listen to the event.
Technical requirements\:
To view this webinar you will need to download the WebEx Application. You will be prompted to download it when you first enter the site. To save time\, you can setup prior to the meeting by following this link\: https\://apidemoeu.webex.com/apidemoeu/meetingcenter/mcsetup.php
Who Should Attend\:
Psychologists\, Psychiatrists\, Social Workers\, Counselors\, Case Managers\, Educators\, Marriage &\; Family Therapists\, Drug and Alcohol Abuse Counselors\, Physicians\, Nurses\, Nurse Practitioners\, Criminal Justice Personnel (Probation Officers)\, Occupational Therapists\, Certified Occupational Therapy Assistants\, Parents
Fed Up with Poor Results from Networking?
Join us for a FREE informative webinar and discover...
Why Networking Doesn’t Work… And What You Should Do About It
We’ve all heard that networking is a great way to grow your business – but are you actually getting your ‘fair share’ of new clients?
• Are you tired of dragging yourself to 7am breakfast meetings and finding the only thing that’s growing is you waistline?
• Do you still dread networking events and go just because you know you ‘should’ go’?
• Is your desk scattered with bundles of business cards from past events but the phone is silent?
Networking ‘should’ bring you tons of new clients!
After all\, it is one of the best marketing strategies you can use to grow your business. Imagine your phone ringing off the hook with prospects requesting your services all from networking. It is possible!
Join us on Thursday\, February 2nd\, at Noon Pacific (2\:00 PM CST\, 3\:00 PM EST\, 8\:00 PM GMT)\, for a 75-minute no-cost webinar full of actionable ideas you can immediately implement.
Discover...
• The 5 most common networking mistakes that are guaranteed to cost you opportunities.
• The number one shift you MUST make if networking is ever going to bring you more prospects.
• A cost effective strategy to leverage your networking efforts and double (or even quadruple!) your success.
• Networking success stories from business owners just like you\, who gained a ton of new clients by networking.
Go to http\://www.sueclement.com/webinar/networking to register and you’ll receive the call information in a personal email from me.
Scheduling conflict? Not sure you can make it? Sign up anyway and you'll get access to the webinar replay.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120203T160000Z DTEND;VALUE=DATE-TIME:20120203T190000Z UID:http://www.webinarcentral.net/content/3-hr-virtual-seminar-safety-how-do-i-get-started-webinar-complianceonline URL;VALUE=URI:http://www.webinarcentral.net/content/3-hr-virtual-seminar-safety-how-do-i-get-started-webinar-complianceonline SUMMARY:3-hr Virtual Seminar - Safety\; How\, Do I Get Started - Webinar By ComplianceOnline DESCRIPTION:This OSHA compliance training will help you understand the importance of getting started as a safety professional and where to start. You will also learn the importance of getting management buy-in.
Description \:
The beginnings of your career in Safety can be intimidating - wondering where to start\, You have been asked if the employees have been trained to operate a piece of equipment and you answer with that confused look\, your insurance company wants the latest OSHA 300 log and you have no idea\, the company president wants the safety committee meeting minutes\, you don’t have one in place – this class will show you where to start.
This 3-hr virtual seminar will equip you with the knowledge and guidance that will allow you to feel secure in your decision making process\, as well as know how to prioritize a day. We will also ensure you know how to handle a worker’s compensation case from start to finish.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120203T180000Z DTEND;VALUE=DATE-TIME:20120203T180000Z UID:http://www.webinarcentral.net/content/art-therapy-and-anxiety-disorders-0 URL;VALUE=URI:http://www.webinarcentral.net/content/art-therapy-and-anxiety-disorders-0 SUMMARY:Art Therapy and Anxiety Disorders DESCRIPTION:This webinar is designed to educate participants about art therapy and provide practical skills for effective assessment and intervention with clients experiencing symptoms of anxiety.
Full Description\:
Practical assessment and intervention skills for treatment of anxiety through art therapy
This webinar is designed to educate participants about art therapy and provide practical skills for effective assessment and intervention with clients experiencing symptoms of anxiety. Demonstrations of art therapy techniques will advance the participants' understanding of the bio psychosocial perspective of many of the disorders that fall under the category of \\"anxiety\,\\" including phobias\, PTSD\, panic\, as well as sleeping and eating disorders. Significant attention will be paid to treatment interventions with numerous opportunities for hands-on art-based techniques.
Course Includes\:
Live Q&\;A
Presentation Handout
Post session recording access
CE Credit
What You Will Learn\:
Discover an alternative method of communicating with clients suffering with anxiety—including PTSD\, Phobias\, Acute Stress\, Eating Disorders\, Sleep Disorders\, and Panic Attacks
Identify effective Art Therapy techniques and learn how to implement them in session
Examine the therapeutic power that art provides in reducing stress and understanding fears
Acquire skills for assessing and treating anxiety
Discuss various art tasks and experience the healing process to promote coping skills in life
Your Presenter\:
PAMELA M. HAYES\, MFT\, LMHC\, ATR-BC\, is an artist and a registered and board certified Art Therapist. She is licensed as a Marriage and Family Therapist and Mental Health Counselor and is currently in private practice in Los Angeles\, California. Ms. Hayes developed the art therapy program at the Rhode Island School of Design–Continuing Education. For the past 15 years\, Ms. Hayes has worked in numerous psychiatric settings with a variety of clients. Currently\, her focus includes families\, couples\, adults and children struggling with mood and anxiety disorders\, addiction\, eating disorders\, abuse and grief-related issues. Ms. Hayes has an undergraduate degree in Fine Arts from Parsons School of Design in New York City and a graduate degree in Marriage and Family Therapy and Art Therapy from Notre Dame de Namur University in Belmont\, California. For more information about Ms. Hayes\, please visit her website at\: www.hayesarttherapy.com.
Disclaimer\:
This event qualifies for one CE credit. Only registered attendees will have access to CE. A Cross Country Education web account is required to attend. There is no charge for a CCE web account. It is recommended that you join the meeting 15 to 20 minutes early. Speaker phone sound quality is poor and it is recommended that they not be used to listen to the event.
Technical requirements\:
To view this webinar you will need to download the WebEx Application. You will be prompted to download it when you first enter the site. To save time\, you can setup prior to the meeting by following this link\: https\://apidemoeu.webex.com/apidemoeu/meetingcenter/mcsetup.php
Who Should Attend\:
Marriage and Family Therapists\, Licensed Professional Counselors\, Social Workers\, Psychiatric Nurses\, Drug and Alcohol Abuse Counselors\, Pediatricians\, Physicians\, Art Therapists\, Pastoral Counselors\, Guidance Counselors\, Youth Pastors\, Youth Counselors\, Educators
This 7-hr virtual seminar on Payroll 201 provides high-level training on topics critical to the intermediate payroll professional. It will increase your knowledge of payroll procedures and compliance regulations beyond the mere basic skills.
Why You Should Attend\:
The payroll professional must deal with rules and regulations from the Department of Labor\, the Internal Revenue Service and the state equivalent of each of these. When you get beyond the basic rules\, the regulations become more complex and demanding. For example\, how to withhold social security taxes is basic. But knowing how to handle social security taxes as it pertains to an overpayment of wages made in previous tax year is quite complex. The payroll professional at the intermediate level must know how to handle this type of situation.
This webinar will help the attendee increase their efficiency and compliance knowledge beyond the basic payroll skills.
Learning Objective\:
The information provided in this program will help the attendee to increase their knowledge of payroll procedures and compliance regulations beyond the mere basic skills. Use of the information presented can significantly increase the attendee’s knowledge in the payroll profession to the intermediate level.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120206T160000Z DTEND;VALUE=DATE-TIME:20120206T170000Z UID:http://www.webinarcentral.net/content/pre-demolition-engineering-survey-webinar-complianceonline URL;VALUE=URI:http://www.webinarcentral.net/content/pre-demolition-engineering-survey-webinar-complianceonline SUMMARY:Pre-Demolition Engineering Survey - Webinar By ComplianceOnline DESCRIPTION:This webinar will help you understand OSHA’s requirement for a pre-demolition engineering survey\, including what documents to have in place\, for renovation and complete demolition of buildings/structures.
Why Should You Attend\:
Due to the significant number of fatalities\, injuries\, fires\, spills/releases\, and “near misses” in construction/demolition activities OSHA requires an engineering survey to be made by a “competent person”. That person may be a professional engineer (PE)\, certified safety professional with demolition experience\, or a demolition contractor employee with adequate experience and communication/writing skills. The survey may be brief for small structures or extensive for large facilities.
Due to unauthorized persons trespassing or accidentally accessing the area and multiple employers working on these projects they are a significant target for lawsuits. Plaintiff attorneys target the failure of conducting\, producing\, and making available a pre-engineering survey.
This webinar will help you understand OSHA’s requirement for a pre-demolition engineering survey for renovation and complete demolition of buildings/structures.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120206T230800Z DTEND;VALUE=DATE-TIME:20020203 UID:http://www.webinarcentral.net/content/autodesk-inventor-2012-essentials URL;VALUE=URI:http://www.webinarcentral.net/content/autodesk-inventor-2012-essentials SUMMARY:Autodesk Inventor 2012\: Essentials DESCRIPTION:Autodesk is a leading manufacturer of 3D design software across a variety of different industries. This course is geared toward students who have the desire to learn the essentials of Autodesk Inventor in order to design models from sketching\, solid modeling\, assembly design\, and drawing production.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120207T160000Z DTEND;VALUE=DATE-TIME:20120207T160000Z UID:http://www.webinarcentral.net/content/understanding-inattentive-adhd-recent-updates-evidence-based-screening-and-treatment-strateg URL;VALUE=URI:http://www.webinarcentral.net/content/understanding-inattentive-adhd-recent-updates-evidence-based-screening-and-treatment-strateg SUMMARY:Understanding Inattentive ADHD\: Recent Updates in Evidence-Based Screening and Treatment Strategies DESCRIPTION:Discover why Inattentive ADHD is different from other types of ADHD and learn the latest information about screening\, SCT\, symptomatology\, comorbidities\, treatment modalities\, medication\, and how this disorder may be mentioned in DSM-5.
Full Description\:
Why is Inattentive ADHD Different? New Information
Attention-Deficit Hyperactivity Disorder\, Predominately Inattentive Type is NOT a “calmer” or “lighter” version of ADHD. The neurophysiology\, symptoms\, treatment methods\, and medications for this disorder are different than the other
types of ADHD. Since patients with Inattentive ADHD are not typically as disruptive as those with other types of ADHD\, this type is commonly misunderstood or goes unrealized by the mental health professional. Little research has been
done compared to Combined ADHD and most seminars and webinars only spend a small portion of time on Inattentive ADHD.
This one-hour course will provide participants with the latest information about screening\, Sluggish Cognitive Tempo (SCT)\, symptomatology\, comorbidities\, treatment modalities\, medication\, and how Inattentive ADHD may be mentioned in
DSM-5.
Course Includes\:
Live Q&\;A
Presentation Handout
Post session recording access
CE Credit
What You Will Learn\:
Identify the differences between Attention-Deficit/Hyperactivity Disorder\, Predominately Inattentive Type (Inattentive ADHD)\, and other forms of ADHD
Define treatment methods for Inattentive ADHD and how such methods are different than those for other forms of ADHD
Outline the common co-morbidities of Inattentive ADHD
Evaluate new research about Sluggish Cognitive Tempo and its relationship to ADHD
Discuss how Inattentive ADHD may be described in DSM-5
Your Presenter\:
KEVIN T. BLAKE\, PhD\, P.L.C.\, is a licensed psychologist and author with over 20 years of experience as a nationally recognized authority on learning disorders and ADHD in children\, adolescents\, and adults. This interest spurred from his
own struggles overcoming a reading disorder/dyslexia and hearing impairment.
Dr. Blake serves as a member of the American Psychological Association\, International Dyslexia Association\, Children and Adults with Attention Deficit Disorders\, Learning Disabilities Association\, and the National Attention Deficit
Disorder Association and was a 1991 delegate to the National Institute for Literacy’s “LEAD 2000 Congress\,” where he advised Congress on diagnostic and remediation issues.
Disclaimer\:
This event qualifies for one CE credit. Only registered attendees will have access to CE. A Cross Country Education web account is required to attend. There is no charge for a CCE web account. It is recommended that you join the meeting
15 to 20 minutes early. Speaker phone sound quality is poor and it is recommended that they not be used to listen to the event.
Technical requirements\:
To view this webinar you will need to download the WebEx Application. You will be prompted to download it when you first enter the site. To save time\, you can setup prior to the meeting by following this link\:
https\://apidemoeu.webex.com/apidemoeu/meetingcenter/mcsetup.php
Who Should Attend\:
Psychologists\, Social Workers\, Licensed Professional Counselors\, Marriage and Family Therapists\, School Psychologists\, Guidance Counselors\, Psychiatric Nurses\, Nurses\, Psychiatric Nurse Practitioners\, Case Managers\, Alcoholism and Drug
Abuse Counselors/Addiction Professionals\, Clergy\, School Administrators\, Physicians\, Psychiatrists\, Mental Health Administrators\, Special Education Teachers\, College Counselors
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120207T180000Z DTEND;VALUE=DATE-TIME:20120207T180000Z UID:http://www.webinarcentral.net/content/key-factors-write-effective-standard-operating-procedure-sop-and-work-instructions-wis-webi-0 URL;VALUE=URI:http://www.webinarcentral.net/content/key-factors-write-effective-standard-operating-procedure-sop-and-work-instructions-wis-webi-0 SUMMARY:Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs) - Webinar By GlobalCompliancePanel DESCRIPTION:This webinar will instruct the participant on how to write\, organize\, and maintain SOPs and train personnel in a way that will ensure compliance in a way that is concise\, reproducible and easy to follow.
It will begin with a strategic view of SOPs in a company and how SOPs can help streamline operations in addition to ensuring regulatory compliance. This will be followed by explanation on how to get from regulations to the SOP. Finally\, Best Practices for creating\, implementing and maintaining SOPs using a risk based approach and getting SOPs ready for inspection will be presented.
Why you should attend\: Standard Operating Procedures (SOPs) are required by law for companies that are regulated by the Code of Federal Regulations such as Title 21 and Title 493. Yet there is no guidance on how to write\, organize and maintain SOPs. Consequently\, SOPs are frequently written in a way that makes compliance difficult or downright impossible. Worse\, this often leads to many regulatory errors that first come to light during an FDA audit.
This webinar will show you how to write\, organize\, and maintain SOPs and train personnel in a way that will ensure compliance in a way that is concise\, reproducible and easy to follow.
Areas Covered In the Session\:
SOPs and their relation to the regulations
SOPs as part of the company's regulatory infrastructure
SOP on SOPs and how to ensure conciseness\, consistency and ease of use
Risk Based approach on SOP Best Practices for creation and maintenance
Training on SOPs
Tools for SOP tracking and when is validation required
What the FDA looks for in SOPs during an inspection
Who will benefit\:
Anyone that creates / maintains SOPs
VP\, Director\, Manager of any dept that writes SOPs or performs training
QA / QC
Regulatory Affairs
Price List\:
Live \: $245.00
Corporate live \: $995.00
Recorded \: $295.00
webinars@globalcompliancepanel.com
http\://www.globalcompliancepanel.com
Phone\: 800-447-9407
Fax\: 302-288-6884
1000 N West Street | Suite 1200 | Wilmington | DE | Zip 19801 | USA
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120207T160000Z DTEND;VALUE=DATE-TIME:20120207T173000Z UID:http://www.webinarcentral.net/content/prepare-tougher-us-fda-cgmp-compliance-audits-webinar-complianceonline URL;VALUE=URI:http://www.webinarcentral.net/content/prepare-tougher-us-fda-cgmp-compliance-audits-webinar-complianceonline SUMMARY:Prepare for Tougher U.S. FDA cGMP Compliance Audits - Webinar By ComplianceOnline DESCRIPTION:This FDA cGMP training webinar will discuss US FDA’s approach to cGMP Audits and expectations from companies. It will also evaluate chief concern areas of cGMP compliance audit and anticipatory emphasis changes as per new regulatory climate.
Why Should You Attend\:
Recent audits indicate the past ways of doing things will no longer be acceptable. Increasingly reports from the field indicate that the Agency is using high-profile cases to drive compliance to smaller companies and suppliers. Recent events in regulated industries indicate a public's growing dissatisfaction with what they view as a lack of oversight of business by regulatory agencies\, including the FDA.
How this is affecting the Agency's approach to audits and their expectations for companies. Pressure on the 510(k) process is only one example. They also use GMP compliance audits to drive companies to do much of their work for them. How they drive companies to do much of their work for them. We will evaluate the chief areas of an FDA CGMP compliance audit to see actual and anticipated changes in emphasis based on this new regulatory climate.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120207T160000Z DTEND;VALUE=DATE-TIME:20120207T160000Z UID:http://www.webinarcentral.net/content/building-global-mindset-webinar-trainhr URL;VALUE=URI:http://www.webinarcentral.net/content/building-global-mindset-webinar-trainhr SUMMARY:Building a Global Mindset - Webinar By TrainHR DESCRIPTION:Overview \: The discussion will include focused discussion on inclusion and diversity and the value add to business activity that comes from using a global mindset to lead teams and the opportunity for creative and innovative thinking that the mindset can foster.
In today's business world it is becoming more important to be able to work effectively across cultures. However a more global mindset is really about building an attitude of inclusiveness so that an organization can not only survive but thrive with the diversity that is growing in our workplaces that include different nationalities but now also includes or will soon include 5 generations. As the world economy staggers and recovers and as we continue to understand how closely all economies of the world are linked\; businesses must understand how a global mindset will assist them.
In our 90 minute program we will explore the topic in three parts and examine what each one involves and why it is important to the future of your business. They are\:
Personal
In the Business
As part of the company culture
The future is more complex and integrated. With a cell phone in almost every hand around the world\, we have more opportunity every day to be more involved in global events. Information that took sometimes years to reach around the world now reaches in second. Just that fact alone changes the way the world interacts. It is important for us to understand the dynamics and impacts of this global information at our fingertips. It is not as easy for media to \\"spin\\" because we can see and hear the immediate truth of the situation. This opens up all kinds of avenues for virtual leadership and management. It depends greatly on a global mindset.
There is tremendous value and opportunity in virtual global management\, when done well. We can learn and grow from understanding how and why things work the way they do in other countries. In that quest\, it is important to be able to make the voice on the other end of the line \\"real\\" and be able to relate to them in a context that is meaningful for us and for them. That is where we can enhance our relationship and opportunities for success.
Areas Covered In the Session\:
Global mindset defined - what does it mean and look like in action
Do I want a global mind set - what is in it for me?
How do I build my own - what can I do to facilitate my personal learning and build my perspective?
How important is a global mindset for my business – what business advantage does it bring to my team? My company?
How do I assist in building an attitude of inclusivity that will nurture a global mindset in my tem? What role do I play in supporting the growth of a global mindset on my team?
Is a global mindset important for my company? Will it be useful and important to our business? How does it contribute to sustainability?
What would a global mindset look like if it was part of our company culture? Do we have to change our values or incorporate a new “attitude” in our values?
How can I assist? How can I contribute?
These learning points will be explored and discussed during the webinar with examples that will support the discussion.
Who will benefit\:
CHRO
Business Leaders (VP)
Risk Managers
A fresh\, innovative approach to Childhood Developmental Disorders
Full Description\:
During this webinar a selection of childhood developmental disorders will be depicted and treatment strategies including medication management will be outlined. Obsessive-Compulsive Disorder and Tic Disorder\, part of a triad of disorders characterized by malfunction of the fronto-striatal circuitry\, will be discussed. PANDAS\, a newly described disorder that can mimic a triad disorder with its symptoms overlapping those of OCD and Tics\, will be introduced and examined. Symptoms of Nonverbal Learning Disabilities will be reviewed and compared with the other disorders. Finally\, brand new\, innovative research on Dysgraphia will be introduced with new methods to help children with handwriting.
Course Includes\:
Live Q&\;A
Presentation Handout
Post session recording access
CE Credit
What You Will Learn\:
Describe the DSM IV criteria for OCD and explain why it is part of the Triad
List the DSM IV criteria for Tic Disorder and explain its role in the Triad
Define NVLD and contrast it with Asperger’s Disorder
Discuss the neurodevelopment of the right hemisphere
Outline the symptoms of Dysgraphia
Your Presenter\:
ANITA REMIG\, Ed.D.\, F.P.P.R.\, F.S.M.I.\, is a practicing clinical psychologist\, certified school psychologist\, and consultant with over 25 years of experience specializing in learning styles\, brain-based research\, and learning problem interventions. Dr. Remig is a member of the American Psychological Association. She is a “Fellow of the Prescribing Psychologist Register” (F.P.P.R.) and a “Fellow in Serious Mental Illness” (F.S.M.I.) from the Prescribing Psychologist Register. Dr. Remig also recently passed the ICCP National Examination for Psychologists in Psychopharmacology and has been awarded a certification as a Medical Psychologist from the Academy of Medical Psychology.
Disclaimer\:
This event qualifies for one CE credit. Only registered attendees will have access to CE. A Cross Country Education web account is required to attend. There is no charge for a CCE web account. It is recommended that you join the meeting 15 to 20 minutes early. Speaker phone sound quality is poor and it is recommended that they not be used to listen to the event.
Technical requirements\:
To view this webinar you will need to download the WebEx Application. You will be prompted to download it when you first enter the site. To save time\, you can setup prior to the meeting by following this link\: https\://apidemoeu.webex.com/apidemoeu/meetingcenter/mcsetup.php
Who Should Attend\:
Psychologists\, Psychiatrists\, Social Workers\, Counselors\, Case Managers\, Educators\, Marriage &\; Family Therapists\, Drug and Alcohol Abuse Counselors\, Physicians\, Nurses\, Nurse Practitioners\, Criminal Justice Personnel (Probation Officers)\, Occupational Therapists\, Certified Occupational Therapy Assistants\, Parents
4 Common Questions include\:
1. What tagging does Attribution require?
2. How do we collect spend data?
3. Can Attribution track emails?
4. How does Attribution determine % of ads seen?
The fact is\, more and more Advertisers &\; Agencies are adding attribution modeling to their media plans for 2012. Knowing the ABC’s of getting up and running and being able to answer questions fashions a smooth start and makes you the expert (Rock Star) at your company meetings.
This free 30-minute webinar will explore how attribution modeling intelligently discerns and quantifies the value of all marketing channels and what steps need to be taken in order to ensure a smooth start.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120207T190000Z DTEND;VALUE=DATE-TIME:20120207T194500Z UID:http://www.webinarcentral.net/content/take-control-your-air-quality-and-multiple-chemical-sensitivities URL;VALUE=URI:http://www.webinarcentral.net/content/take-control-your-air-quality-and-multiple-chemical-sensitivities SUMMARY:Take control of your Air Quality and Multiple Chemical Sensitivities DESCRIPTION:MCS (Multiple Chemical Sensitivity) can affect people of all ages and backgrounds. It is characterized by extreme sensitivities and allergic-type reactions to even the slightest trace of chemicals.
In this webinar\, we will explore the many facets of Indoor Air Quality and we will present easy ways to make the Indoor Air Environment healthier and safer for people afflicted with MCS symptoms\, with simple yet effective steps.
• What is an MCS Air Quality Program
• Sources of Poor IAQ
• How can Pollutants Affect Me
• Simple\, Sound Solutions
• Overview of Air Cleaning Technologies
• Advantages of a Healthy Indoor Environment
• Benefits of Cleaner Air
A little public relations savvy can get you valuable media coverage. Coverage that has more impact than any advert you can buy. Attend this webinar to learn\:
The power of no cost publicity and how to get it.
What stories the media want to cover.
How to target the right media.
How to write a media release.
Media interview tips.
How to use free publicity to grow your brand.
One media success often leads to another. Learn how to get the publicity ball rolling for you at this webinar.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120208T140000Z DTEND;VALUE=DATE-TIME:20120208T170000Z UID:http://www.webinarcentral.net/content/medical-device-process-validation-statistical-considerations-webinar-complianceonline URL;VALUE=URI:http://www.webinarcentral.net/content/medical-device-process-validation-statistical-considerations-webinar-complianceonline SUMMARY:Medical Device Process Validation - Statistical Considerations - Webinar By ComplianceOnline DESCRIPTION:This Process Validation training will look at the underlying statistical concepts to perform an effective process validation. The webinar examine elements of the FDA regulations for process validation (21 CFR §820.75) as well as the corresponding requirements in ISO 13485.
The FDA’s Quality system regulation requires device manufacturers to validate processes when they don’t fully verify the resulting output. Based on Warning Letters\, the FDA expects manufacturers to validate processes when the output check uses sampling instead of 100% inspection.
The presentation looks at these aspects of process validation using the unifying approach of a statistical model. Rather than a fundamental examination of how to perform process validation\, this seminar covers the tools necessary to use the statistical model.
Why Should You Attend\:
If you conduct process validation\, you need to ensure that your results are valid. Beyond the regulatory requirements\, statistical approaches will help you achieve the desired result – processes that produce only conforming material. This is the essence of the statistical approach.
This Listeria Prevention training will cover HAACP requisites as well as GMP and Sanitation programs to address areas of possible listeria contamination and methods to eradicate them.
Why Should You Attend\:
With the crisis we have seen in food safety in the last decade\, deli meat\, cheeses\, sprouts\, cantaloupe etc\, QC managers are under a lot of pressure to maintain a clean sanitized facility while focusing on their HAACP plan and other crucial responsibilities. The potential for cross contamination occurs in the facility every day. Finished product is often too close to other adulterants or the adulterants can be human!
This presentation will help a QC manager of a RTE processor to look through the “lens” of their HAACP and other prerequisite building blocks like strong GMP and Sanitation programs. We’ll help you see areas that the facility may be weak in and show you some tools to address\, particularly sanitation\, where the areas of possible listeria can be hiding\, and how to clean well enough to eradicate them.
Learning Objectives\:
Attendees will learn more about the keys to preventing listeria in the processing environment\, take an in depth look at a strong sanitation program.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120208T160000Z DTEND;VALUE=DATE-TIME:20120208T173000Z UID:http://www.webinarcentral.net/content/setting-effective-internal-audit-program-webinar-complianceonline URL;VALUE=URI:http://www.webinarcentral.net/content/setting-effective-internal-audit-program-webinar-complianceonline SUMMARY:Setting up an effective Internal Audit Program - Webinar By ComplianceOnline DESCRIPTION:This 90-minute Internal Audit webinar will cover the three foundational elements that support an effective Internal Audit program - establishing Internal Audit Program objectives\, developing audit plans\, and writing effective non-compliances.
Why Should You Attend\:
Internal auditing drives continual improvement and reminds everyone that Quality comes first! Auditing is an assessment tool that provides a reliable performance indicator of your organization’s system and processes. In other words\, an internal audit is an audit of an entity's internal control systems and procedures and how the system and procedures are implemented. Companies that establish internal audits as part of their culture to practice discipline of process control will benefit in the long run with stable and reliable processes.
In 90 minutes we will cover three foundational elements for designing an effective internal audit process. These areas include how to establish Internal Audit Program objectives\, develop audit plans\, and write effective non-compliances.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120209T170000Z DTEND;VALUE=DATE-TIME:20120209T170000Z UID:http://www.webinarcentral.net/content/kpi-definition-business-activity-monitor-20 URL;VALUE=URI:http://www.webinarcentral.net/content/kpi-definition-business-activity-monitor-20 SUMMARY:KPI definition with Business Activity Monitor 2.0 DESCRIPTION:Different groups within an organization need to monitor different Key Performance Indicators (KPIs) - An operations team will be interested in the response times of business services and loads of each service\, while members of a business unit will be interested in sales per day\, sales trends by hour per day etc. The diverse requirements of each group would potentially result in countless hours spent on customizing a solution.
This session provides a demonstration of BAM 2.0's value as a monitoring framework. In particular we will observe how the analytics framework and WYSIWYG UI generation tools can be customized to monitor a retail store use case and a system operations use case without spending hours of development time.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120209T160000Z DTEND;VALUE=DATE-TIME:20120209T170000Z UID:http://www.webinarcentral.net/content/life-cycle-validation-gmp-potency-bioassays-webinar-complianceonline URL;VALUE=URI:http://www.webinarcentral.net/content/life-cycle-validation-gmp-potency-bioassays-webinar-complianceonline SUMMARY:Life Cycle Validation of GMP Potency Bioassays - Webinar By ComplianceOnline DESCRIPTION:This 90-minute webinar will provide guidelines for bioassay validation and regulatory documentation\, the steps for technology transfer and commercial validation show how to implement the new USP chapters 1032\, 1033 and 1034.
Why Should You Attend\:
Potency bioassays are an integral part of release testing and stability studies for biotechnological products. There is a lack of clarity of how much work is required at each development phase to maintain scientific rigor and meet regulatory expectations.
This webinar provides a logical plan to progress the potency bioassay from a tool to assist in pre-clinical process evaluation throughout final commercial implementation. The presentation provides strategies to comply with current regulatory guidance like the new USP chapters for bioassay potency (USP 1032\, USP 1033 and USP 1034) and discusses options to determine acceptance parameters not only for the precision\, parallelism and accuracy of the method but also for the potency of each sample. The participants in this webinar will learn a common sense chronological pathway that can easily be adapted to the successful fit-for-purpose validation of any biopharmaceutical method.
Areas Covered in the Seminar\:
- Rational approaches to bioassay selection and optimization.
- Effective transition of bioassays from early to late stage product development.
- Strategies to increase accuracy and repeatability.
- Techniques to avoid common technical problems.
- Guidelines for bioassay validation and regulatory documentation.
- Steps for preparing a method for technology transfer and commercial validation.
- Implementation of USP 1032\, 1033 and 1034.
This 4-hr training will address both the legal and psychological issues that often arise while dealing with Psychiatric Disabilities at Work. You will learn to deal with sensitive and challenging scenarios and directly address mental health problems with managers and employees.
Why Should You Attend\:
The recent amendments to the A.D.A. have a significant impact on the rights of mentally employees as well as the responsibilities of employers. To make matters more confusing\, the A.D.A.\, the F.M.L.A.\, and worker’s comp can intersect\, or supersede\, each other when it comes to dealing with psychiatric disabilities.
This intermediate to advanced\, 4 hour workshop will enable HR professionals to navigate the difficult and often murky challenge of dealing with \\"invisible disabilities.\\"
This practical workshop address both the legal and psychological issues that often arise\, such as confidentiality\, fitness for duty evaluations\, relevant laws\, drug testing\, the relationship between conduct problems and mental illness\, and how to directly address mental health problems with managers and employees.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120209T160000Z DTEND;VALUE=DATE-TIME:20120209T200000Z UID:http://www.webinarcentral.net/content/4-hr-virtual-seminar-latin-america-regulatory-compliance-requirements-life-science-products URL;VALUE=URI:http://www.webinarcentral.net/content/4-hr-virtual-seminar-latin-america-regulatory-compliance-requirements-life-science-products SUMMARY:4-hr Virtual Seminar - Latin America\: Regulatory Compliance Requirements for Life Science Products DESCRIPTION:This 4-hr Latin America Regulatory compliance requirements training/webinar will cover topics relating to pre-clinical and clinical requirements\, as well as\, addressing the structure of the regulatory agencies in Latin America.
Why Should You Attend\:
This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals\, Medical Devices\, Biologics and Combination Products in Latin America. The primary countries covered will include\: Argentina\, Brazil and Mexico. Other countries such as Chile\, Costa Rica\, Dominican Republic\, Panama\, Peru and Venezuela will be discussed. The course will cover topics relating to pre-clinical and clinical requirements\, as well as\, addressing the structure of the regulatory agencies in Latin America. Content will include descriptions of the methods by which regulators in the corresponding agencies process filings and registrations and what is expected in the authorization and dossier maintenance of licensed products.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120209T160000Z DTEND;VALUE=DATE-TIME:20120209T170000Z UID:http://www.webinarcentral.net/content/purposeful-water-and-steam-system-validation-%E2%80%93-not-just-regulatory-requirement URL;VALUE=URI:http://www.webinarcentral.net/content/purposeful-water-and-steam-system-validation-%E2%80%93-not-just-regulatory-requirement SUMMARY:Purposeful Water and Steam System Validation – Not Just A Regulatory Requirement DESCRIPTION:This Water system validation training will guide you how validation should be customized to your particular water system design and maintenance practices\, what operational elements should be included in the microbial testing during validation and which ones need not be. Understanding the purpose of water system validation will allow you to see the fallacies of many standard protocol templates bred by tradition and do only what is appropriate for YOUR water system.
Why Should you Attend\:
- Are you sure your water system was properly validated?
- Have you ever had chemical or microbial control problems with the water system that did not show up during validation?
- Have those problems ever caused manufacturing interruptions?
- Have those problems ever caused product problems? Are you absolutely sure?
Though FDA is often glad to see that any sort of water system validation has been done\, they will quickly raise their expectations (and \\"483 pad\\") if your validation was poorly done and resulted in product/health problems. You can avoid this regulatory attention as well as these product problems by applying a little logic to your validation protocol and avoiding standard templates which may not be the right challenge for YOUR water system. However\, to apply logic\, you MUST understand how your water system is intended to work and what could make it fail to do so. With every water system being different\, a customized validation protocol is a necessity. Attending this presentation will allow you to understand what water system features are essential to include in validation (and which are not)\, and will also explore the validation needs of laboratory water systems as well as issues related to supposedly cost-avoiding options like using package waters.
“Building an Engaged Campus\,” will be held on February 9 at 11am PT (2pm EST) and led by Alan Cattier\, Director of Academic Technology Services at Emory University. Cattier will offer best practices from 15 years of using social technologies in education at Emory University and share his vision for building a vibrant\, more engaged campus.
• Learn how social technologies are being utilized to help streamline communications &\; foster student engagement
• Discuss the emerging role of Private Academic Social Networks\, and how they differ from Facebook and Twitter
• Discover how to transform static portals into \\"intelligent activity streams\\" that ensure that you get the right information to the right people in the right way
• Explore new tools for fostering connections and collaboration between colleagues\, cohorts and classmates
• Learn how students\, faculty and staff can benefit from a connected campus
For more information\, please visit www.goingon.com/emory-webinar
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120209T170000Z DTEND;VALUE=DATE-TIME:20120209T170000Z UID:http://www.webinarcentral.net/content/suicide-loss-what-all-medical-professionals-should-know URL;VALUE=URI:http://www.webinarcentral.net/content/suicide-loss-what-all-medical-professionals-should-know SUMMARY:Suicide Loss\: What All Medical Professionals Should Know DESCRIPTION:Led by an experienced therapist in the field\, this webinar outlines the complex issues faced by survivors of suicide and provides medical and behavioral health professionals with treatment strategies for individuals at all stages of
recovery.
Full Description\:
Every 15 minutes someone in the United States dies by suicide\, leaving behind 6-8 loved ones\, known as survivors of suicide. The word suicide continues to be associated with shame and stigma\, leaving many individuals who need mental
health treatment and those left behind by suicide afraid to reach out for help. Many survivors hold a lot of their feelings and thoughts inside\, even while seeking treatment.
The complexity of suicide and suicide loss leave many professionals feeling under-educated and ill-prepared to work with a survivor in treatment. Led by an experienced therapist and specialist in the field\, this webinar is designed to
investigate the complex grieving process associated with this loss and to provide new strategies for working with individuals at all stages of recovery. Ms. Falasco brings both her extensive training in prevention and postvention to this
webinar\, as well as her personal experiences as a suicide survivor.
Course Includes\:
Live Q&\;A
Presentation Handout
Post session recording access
CE Credit
What You Will Learn\:
Identify the effects of suicide loss on survivors and helpers
Examine the current statistics on suicide and the nature of suicide
Identify grief reactions\, grieving styles\, and symptoms of traumatic grief
Describe the nature\, process\, and phases of suicide loss
Describe suicide postvention measures and loss support resources available to survivors
Learn specific interventions and techniques to assist the survivor through the mourning process
Your Presenter\:
Linda Falasco\, LCSW\, a licensed clinical social worker with over 20 years of experience. Ms. Falasco is a graduate of Temple University with a Masters in Social Work and has extensive post-masters training in child development\, play
therapy\, and bereavement. A seasoned lecturer on suicide loss\, Ms. Falasco brings both her extensive training in prevention and postvention to this webinar\, as well as her personal experiences as a suicide survivor.
Disclaimer\:
This event qualifies for one CE credit. Only registered attendees will have access to CE. A Cross Country Education web account is required to attend. There is no charge for a CCE web account. It is recommended that you join the meeting
15 to 20 minutes early. Speaker phone sound quality is poor and it is recommended that they not be used to listen to the event.
Technical requirements\:
To view this webinar you will need to download the WebEx Application. You will be prompted to download it when you first enter the site. To save time\, you can setup prior to the meeting by following this link\:
https\://apidemoeu.webex.com/apidemoeu/meetingcenter/mcsetup.php
Who Should Attend\:
Clergy\, Counselors\, Drug and Alcohol Counselors\, Educators\, Hospital (Clinical)\, Long-Term Care (Clinical)\, Marriage and Family Therapists\, Nurse Practitioners\, Psychologists\, Social Workers
Hear about the latest trends surrounding this relatively new method for marketing your business.
What it means to go mobile
How consumers actually use mobile
Will Mobile Marketing really work in my business?
Mobile Websites vs Mobile Apps\: How to decide
How to get your marketing message read over 90% of the time
QR codes - everything you need to know about them!
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120210T160000Z DTEND;VALUE=DATE-TIME:20120210T173000Z UID:http://www.webinarcentral.net/content/affirmative-action-and-recent-trends-within-ofccp-webinar-complianceonline URL;VALUE=URI:http://www.webinarcentral.net/content/affirmative-action-and-recent-trends-within-ofccp-webinar-complianceonline SUMMARY:Affirmative Action and Recent Trends within the OFCCP - Webinar By ComplianceOnline DESCRIPTION:This 90-minute training will discuss recent OFCCP enforcement trends and regulatory initiatives and review these against your current practices and procedures to ensure your company is audit ready. It will also cover the proactive steps that federal contractors can take to prepare for the impending rules.
Why Should You Attend\:
In this session\, we will review the recent OFCCP enforcement trends and regulatory initiatives. Attendees will learn about OFCCP latest regulatory developments such as the Agency’s new enforcement methods for analyzing compensation and its Active Case Enforcement initiative. We will discuss the new proposed affirmative action regulations for individuals with disabilities\, the new wave of scheduling letters\, as well as other actions that highlight OFCCP’s stepped-up enforcement as they work collaboratively and aggressively with the Solicitor’s Office.
This webinar is critical for employers who want to stay up-to-date with current OFCCP developments in order to avoid potential violations during an OFCCP audit.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120210T160000Z DTEND;VALUE=DATE-TIME:20120210T180000Z UID:http://www.webinarcentral.net/content/does-your-pharmaceutical-lab-have-gmp-and-non-gmp-functions-webinar-complianceonline URL;VALUE=URI:http://www.webinarcentral.net/content/does-your-pharmaceutical-lab-have-gmp-and-non-gmp-functions-webinar-complianceonline SUMMARY:Does your pharmaceutical lab have GMP and non-GMP functions? - Webinar By ComplianceOnline DESCRIPTION:In this 2-hr webinar you will learn how to differentiate and draw boundaries for GMP and GLP practices if done in same laboratory and how to transition a procedure in development to one used routinely.
Why Should You Attend\:
If a laboratory is dedicated either to GMP testing and validation activities or to method and procedure development and validation\, then the laboratory is responsible for following the appropriate CFRs. GMP guidance’s for the pharmaceutical industry are included in 21 CFR\, and for GLP guidance’s can be found in 58 CFR. However\, if both types of work are being done in the same laboratory and even by the same analysts\, it is critical to define boundaries. This involves not only the analysts and the laboratory management but extends to reviewers of critical documents and client education regarding the practices and policies.
Attend this 2-hr presentation webinar with your team to understand the pitfalls and risks of having GMP and GLP practices occurring in one location and strengthen the understanding of the lifecycle of a method or procedure.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120210T160000Z DTEND;VALUE=DATE-TIME:20120210T190000Z UID:http://www.webinarcentral.net/content/managing-osha-inspections-and-accident-investigations-webinar-complianceonline URL;VALUE=URI:http://www.webinarcentral.net/content/managing-osha-inspections-and-accident-investigations-webinar-complianceonline SUMMARY:Managing OSHA Inspections and Accident Investigations - Webinar By ComplianceOnline DESCRIPTION:This OSHA Inspection and Accident Investigation training will provide practical tips for safety professionals and managers on what the OSHA inspectors will look for\, how to respond to a letter of complaint\, how employees and unions figure into the inspection equation\, and what you must do to expedite the inspection and help resolve issues before they become major problems.
Why Should You Attend\:
Perhaps of all of the interactions that occur with regulatory agencies\, the unannounced OSHA inspection is the most stressful\, and least understood by business owners. The key to managing a surprise OSHA Inspection or a letter of complaint directed at your company is to understand what the process is and what the OSHA inspectors are looking for.
This presentation will explain what the process is for an OSHA inspection\, and how to respond to a letter of complaint. Also\, this presentation will explain what inspectors are looking for\, how employees and unions figure into the inspection equation \, and what you must do to expedite the inspection and help resolve issues before they become major problems.
This session will help business owners and safety personnel have a better understanding and feel more in control of the situation when OSHA inspectors arrive at your site\, especially if they arrive unannounced.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120210T180000Z DTEND;VALUE=DATE-TIME:20120210T190000Z UID:http://www.webinarcentral.net/content/planning-your-first-webinar-what-why-and-how-make-it-success URL;VALUE=URI:http://www.webinarcentral.net/content/planning-your-first-webinar-what-why-and-how-make-it-success SUMMARY:Planning Your First Webinar - The What\, Why and How to Make it a Success DESCRIPTION:Creating effective webinars takes planning\, organizational skills\, diplomacy and specialized expertise. This 45 minute educational webinar discusses what it takes to plan\, prepare and host webinars as part of a business or member outreach program.
Attend this interactive webinar to learn\:
• Each step in the webinar planning process - Identify all of the elements needed - from speaker selection to post-event follow-up - to produce professional webinars.
• Guidelines to evaluating vendor options - Learn the difference between webinar technology providers.
• Simple marketing tasks that drive webinar attendance - Discover the latest techniques to find and market to your audience.
You should only attend if you are an administrator\, marketer or moderator who supports business or organizational webinars. All attendees will receive a FREE \\"How to Produce a Profitable Webinar\\" white paper which includes an easy-to-follow implementation and planning guide.
If you can’t attend the webinar\, register anyway\, and we will send you a link to a free replay.
About the Presenter\:
Don Cameron\, Marketing Strategist and founder of Interactive Telesis and ConferTel\, has helped hundreds of organizations generate non-dues revenue by delivering educational webinars to their members in addition to helping businesses use an educational marketing approach to cost-effectively generate qualified sales leads.
This webinar will give a good understanding of USP and FDA requirement and provide recommendations and tools for effective implementation.
Compendial methods such as USP and EP standards are validated by the organizations that have developed and published the method. The FDA requires users of such methods to demonstrate the user's competence to successfully run the method. For example\, 21 CFR 211.194 (a) states\: The suitability of all testing methods used shall be verified under actual conditions of use. However\, the FDA does not give any further guidance on what\, when and how. And the first revision of USP <\;1226>\; did not have specific recommendations. But FDA inspectors got out and write 483's and warning letters related to <\;1226>\;. Now USP has announced to come out with a new revision using the risk based approach for the type and extend of testing.
Reference material for easy implementation\:
SOP\: Verification of Compendial Methods
Checklist\: - Verification of Compendial Methods
Case Studies\; Verification of Compendial methods and Procedures
Areas Covered in the Session\:
What are FDA and international requirements for compendial methods?
What and how much should be tested?
How to use the risk based approach?
Is system suitability testing enough?
Do all compendial routine methods require verification?
When could just system suitability testing be enough?
Should we verify all performance characteristics?
How much can we deviate from the compendial method without the need for a full revalidation?
What to do if the compendial procedure cannot be verified?
How frequently should compendial methods be re-verified?
What if our equipment was not included in the USP method validation experiments
Who Will Benefit\:
Analysts
Lab Supervisors and Managers
QA managers and personnel
Analysts
Consultants
Teachers
Price List\:
Live \: $245.00
Corporate live \: $995.00
Recorded \: $295.00
webinars@globalcompliancepanel.com
http\://www.globalcompliancepanel.com
Phone\: 800-447-9407
Fax\: 302-288-6884
This webinar on addressing fungal and bacterial spore outbreaks will discuss case studies on excursion investigations and show how facility design\, personnel practices and cleaning and disinfection effect excursion investigations.
Why Should You Attend\:
This presentation will show how you can effectively troubleshoot fungal and bacterial spore outbreaks. Case studies on excursion investigations will be described and discussed in detail. We will also cover disinfectant efficacy testing present data on different biocidal products and actives.
The speaker will present and discuss examples of contamination issues which were investigated and resolved after several weeks of troubleshooting.
Areas Covered in the Seminar\:
Learn ways to review environmental monitoring data.
Discuss case studies on excursion investigations.
Learn how facility design\, personnel practices and cleaning and disinfection effect excursion investigations.
Discuss worst case events that can cause excursions
Register for this free webinar to learn about common contaminants\, possible health effects and simple solutions!
Salon and spa workers\, owners and patrons often have to deal with poor air quality\, which can affect their health and well-being.
During this webinar\, you will discover the most common causes of poor indoor air quality in spas and salons\, which products or substances to be careful about\, fascinating industry statistics and facts as well as a discussion of possible solutions and technologies.
With federal agencies like OSHA and the FDA honing in on formaldehyde exposure and other occupational health and safety concerns\, this information can make the difference in your establishment.
Sign up now to reserve your spot\; we look forward to seeing you there!*
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120214T160000Z DTEND;VALUE=DATE-TIME:20120214T170000Z UID:http://www.webinarcentral.net/content/fdas-current-thinking-industry-cgmps-phase-1-inds URL;VALUE=URI:http://www.webinarcentral.net/content/fdas-current-thinking-industry-cgmps-phase-1-inds SUMMARY:FDA's Current Thinking for Industry cGMPs for Phase 1 INDs DESCRIPTION:This US FDA draft guidance documentation webinar/ training will give an insider’s insight into the new guidance and regulation and discuss the rationale for such.
Description
The US FDA has issued a draft guidance document outlining a suggested approach to complying with current good manufacturing practice (CGMP) requirements for drugs intended soley in Phase 1 studies.With this guidance and an accompanying regulation\, US FDA formally recognizes specific standards for the manufacture of small amounts of drug products for phase 1 studies and formulating an approach to cGMP compliance that is appropriate for the particular stage of drug development. This presentation will give an insiders insight into the the new guidance and regulation and discuss the rationale for such.
Areas Covered in the seminar\:
- Background and rationale for guidance and proposed regulation
Scope
- CGMP Statutory and Regulatory Requirements
- Recommendations for complying with the statue- personnel\,Quality Control Function\, facility and Equipment\, Control of Components\, Production and Documentation\, -Laboratory Controls\,Container Closure and Labeling\, Distribution and Record keeping
- Special production situations
- Biological and Biotechnological Products
- Sterile products/aseptically processed products
- Questions
Overview \: You cannot manage productivity with an appraisal form. Learn to define performance as a three legged stool that ensures everything that matters is managed. Some employees perform well but poison the environment around them.
Team members might resent or even undermine group efforts when one individual's bad behavior is tolerated. Others try hard but fail. Only through a holistic approach to performance can maximum productivity be achieved. Therefore\, managing what individuals do everyday\, tracking the results that come from their contributions\, and including how they work with others are all necessary to ensure performance success. Make sure that employees are the first step in the quality assurance process.
Learn how to train employees to indentify the key variables that identify success. Build a support system that does not allow employees to fail\, languish\, or to waste time on unproductive tasks. Instead of asking employees to show up for 8 hours a day\, design a work environment that challenges them to do their very best work each day. Unleash employee excitement and potential by getting them involved\, supporting them\, and directing them in a new and novel way that respects that talents and abilities of today's knowledge workers.
Why you should attend\: When does a focus on results undermine productivity? Can employees complete the right way and on time but unintentionally sabotage the organization? Do managers sometimes ignore ticking time bombs that poison the area around them by not dealing with behavioral issues? The only way to be an effective manager is to manage performance holistically by balancing the focus on efforts\, outcomes\, and behaviors. Learn how to ensure that each assignment\, your supervisor techniques\, your performance management system\, and your compensation system are all aligned and support the kind of performance that you produce lasting results. Don't pay employees to get results and allow them to cannibalize future sales. Hold employees accountable for what they do\, what they fail to do\, and how they do it. Ensure that the work smart\, safe\, efficiently and effectively. Do not allow employees to cut corners\, undermine coworkers\, or fail to follow policies and procedures. Build a performance management system and performance management system that complement one another and ensure that each employee is held to high standards.
Areas Covered in the Session\:
Define what excellent performance \\"looks like\\" from the employee's perspective
Diagnose performance problems effectively
Select the proper management intervention to correct poor performance
Use the right management tools to keep employees on track
Train managers to help employees be more productive
Review or revamp your performance management system
Ensuring Incentive Plans are designed to support the \\"actual\\" results you seek
Who Will Benefit\:
Managers
Supervisors
HR Managers
Directors
Coordinators
Vice Presidents
his presentation will cover the scope\, status and results of the surveillance inspections and what they may mean for the future of 21 CFR Part 11. This will enable you to determine whether your company is subject to the most common violations so you can take action to have a better inspection outcome.
In December 2010 FDA started the Part 11 inspection initiative. While originally the initiative was supposed to last 3-6 months\, it has now turned into an ongoing program with Part 11 related issues being part of most future inspections. At the beginning of the initiative FDA made it very clear that Part 11 is in effect and is enforced according to the original Part 11 and the Guidance from 2003. In the meantime FDA officials reported about key findings. For example\, George Smith who heads up FDA's Part 11 working group gave an update with examples of violations.
Why you should attend\: In December 2010 the FDA changed the way it does audits to include 21 CFR 11 add-on inspections. Very little is known about this\, yet the FDA has already issued citations on the subject. This Webinar will present the latest on FDA thinking (with slides directly from the FDA's Office of Compliance)\, discuss how these inspections will impact both your company and the industry\, and provide guidance on how your company can ensure that they have a successful inspection.
Areas Covered In the Session\:
What is FDA's most current thinking related to computers and electronic records?
What are the inspection trends?
What are most frequent recent citations for Part11?
What are the most frequent deviations for computer system validation?
Under which circumstances can inspectors exercise enforcement discretion?
How important is risk based Part11 compliance?
Who will benefit\:
Everybody using computers in FDA Regulated Environments
IT Manager and Staff
QA Managers and Personnel
Regulatory Affairs
Training Departments
Consultants
Validation Specialists
Price List\:
Live \: $245.00
Corporate live \: $995.00
Recorded \: $295.00
webinars@globalcompliancepanel.com
http\://www.globalcompliancepanel.com
Phone\: 800-447-9407
Fax\: 302-288-6884
1000 N West Street | Suite 1200 | Wilmington | DE | Zip 19801 | USA
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120214T160000Z DTEND;VALUE=DATE-TIME:20120214T173000Z UID:http://www.webinarcentral.net/content/when-fmla-ends-and-ada-begins-fmlaada-crossover-coordination-management-and-compliance-strat URL;VALUE=URI:http://www.webinarcentral.net/content/when-fmla-ends-and-ada-begins-fmlaada-crossover-coordination-management-and-compliance-strat SUMMARY:When FMLA ends and ADA begins. The FMLA/ADA Crossover\: Coordination\, Management\, and Compliance Strategies DESCRIPTION:This 90-minute training will assist you in understanding the complex interaction between FMLA and ADA (AA) as it relates to intermittent leave requests with an underlying accommodation. In addition\, we will clarify and discuss strategies for managing the transition from FMLA to ADA\, concurrent ADA compliance requirements when designating FMLA\, and the significant differences between the compliance requirements.
Description
Do you refrain from terminating employees because you are concerned about running afoul with either the FMLA or ADA and do not want a lawsuit? This interactive Webinar workshop will help you understand when and how you can have confidence to terminate employees if they are not complying with notification and intermittent leaves as they relate to both FMLA and the ADA. Learn when enough is enough\, and how to clearly document the process to avoid costly lawsuits.
This webinar provides an overview of areas in which the biggest mistakes are made. It is an opportunity for HR and Payroll professionals to learn strategies for consistent application of compliance regulations. We will cover the significant differences between the FMLA and ADA notification process and the medical certification documentation required to determine eligibility for leave. We will also explain the difference between notification\, required documentation and the confirmation of your company’s ability to accommodate without undue hardship. This webinar will introduce simple compliance strategies\, to help you clearly understand the intent of both the FMLA and ADAAA when accommodating requests for intermittent leave that include a request for an accommodation.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120214T160000Z DTEND;VALUE=DATE-TIME:20120214T164500Z UID:http://www.webinarcentral.net/content/iaq-ii-challenges-office-%E2%80%93-indoor-air-quality-management URL;VALUE=URI:http://www.webinarcentral.net/content/iaq-ii-challenges-office-%E2%80%93-indoor-air-quality-management SUMMARY:IAQ II - Challenges at the Office – Indoor Air Quality Management DESCRIPTION:Indoor Air Quality Challenges at the Office
A healthy workplace starts with healthy air
A majority of workers spend 40 or more hours at the office – and poor indoor air quality can affect their performance\, productivity and well-being\, which in turn can hurt a company’s bottom line.
In this webinar\, we explore common aspects of IAQ and offer an in-depth analysis relating to air quality and the need for proper indoor air management to avoid health hazards and related complications.
Find out what you can do to improve the indoor air quality in your workplace\, what questions to ask and how a healthier work environment can benefit the employees as well as the company.
We will propose an effective\, preventive IAQ management program that addresses many areas\, including source control – ventilation – humidity control – filtration.
Join us in Part II of our Webinar Series on IAQ Management at the workplace!
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120214T211500Z DTEND;VALUE=DATE-TIME:20120214T211500Z UID:http://www.webinarcentral.net/content/small-biz-success-summit URL;VALUE=URI:http://www.webinarcentral.net/content/small-biz-success-summit SUMMARY:Small Biz Success Summit DESCRIPTION:Want to know how to create a blog that provides ongoing streams of traffic and fuels the growth of your business? During this session\, the founders of four top blogs will share how they've built multimillion-dollar empires by producing regular and valuable content for their blogs. You'll discover how they started\, what to avoid\, and how they use their blogs to drive sales. You'll also have an opportunity to ask your questions live to our panel. Lee will be presenting on a panel with Brian Clark\, Joe Pulizzi\, and Mike Stelzner
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120215T160000Z DTEND;VALUE=DATE-TIME:20120215T170000Z UID:http://www.webinarcentral.net/content/cro-or-aro-how-hire-and-manage-one-webinar-complianceonline URL;VALUE=URI:http://www.webinarcentral.net/content/cro-or-aro-how-hire-and-manage-one-webinar-complianceonline SUMMARY:CRO or ARO\: How to Hire and Manage One - Webinar By ComplianceOnline DESCRIPTION:Why Should You Attend\:
A critical component in successful Clinical Research Trials is ensuring that you choose the right CRO/AOR based on the phase of the trial\, the therapeutic area and the countries that the trials will be conducted. It is then important that the scope of the work be clearly defined to ensure that budget and timelines are respected and that the data collected will stand up to regulatory scrutiny. This protects both the CRO/ARO and the sponsor company. It also makes the job of the Project Managers on both sides easier.
This presentation will show how you can manage the CRO/ARO in this environment of multi-center\, multi-country trials. We will discuss how you can ensure that you comply with regulations in the various countries from shipping drug to ensuring that the inclusion criteria are well understood in all countries and that the appropriate patients are enrolled. Diagnostic criteria are not always interpreted in the same manner. This is particularly true in some therapeutic areas such as CNS. We will also review the current trend towards enrolling pediatric patients as well as elderly and more vulnerable populations\, and the challenges that go with it\, in the various environments that studies are conducted.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120215T160000Z DTEND;VALUE=DATE-TIME:20120215T173000Z UID:http://www.webinarcentral.net/content/environmental-monitoring-and-contamination-control-plan-webinar-complianceonline URL;VALUE=URI:http://www.webinarcentral.net/content/environmental-monitoring-and-contamination-control-plan-webinar-complianceonline SUMMARY:Environmental Monitoring and Contamination Control Plan - Webinar By ComplianceOnline DESCRIPTION:This 90-minute cleanroom contamination control training will review the common mistakes that people make in cleanrooms that lead to contamination\, show how to develop a successful contamination control program and discuss ways to improve your facility's design and maintenance.
Why Should You Attend\:
This 90-minute presentation will review the basics of personnel practices and discuss cleaning and disinfection. The most common source of contamination in the cleanroom are people and as such it is important to cover common mistakes in behavior and gowning. The speaker will address facility design and conditions as well since these are also a contributor to contamination. As an attendee\, you will get a complete overview the basics of how to control your cleanroom environment how to get the best possible yield of products.
Areas Covered in the Seminar\:
- Review the most common mistakes people make in cleanrooms that lead to contamination.
- Learn how to develop a successful contamination control program.
- Learn ways to improve facility design and maintenance.
This one-hour webinar is designed to educate participants on how to guide clients through the process of describing their art work in order to understand patterns of behavior and ways to self-soothe.
Full Description\:
Evoke insight and understanding for your clients through their art work!
This webinar is designed to educate participants on how to ask open-ended questions to facilitate communication after clients have created the art work. Precise questions to be asked of the client will be provided based on specific art techniques. Participants will be discouraged from imposing their own interpretations on their clients' art work and will be guided on how to get clients to open up when describing their art-making experiences. This webinar will also provide specific techniques as well as the language needed to describe the directives. In addition\, you will learn what questions to ask that will best evoke insight and understanding from the client regarding unconscious motivations\, patterns of behavior\, and ways to self-soothe.
Course Includes\:
Live Q&\;A
Presentation Handout
Post session recording access
CE Credit
What You Will Learn\:
Discover an alternative method of communicating with clients
Examine effective Art Therapy techniques and learn how to implement them in session
Recognize the therapeutic power that art provides\, and how to affectively use the art as a means of communication
Identify skills for assessing and treating a multitude of clients
Discuss various art tasks and experience the healing process to promote coping skills in life
Your Presenter\:
PAMELA M. HAYES\, MFT\, LMHC\, ATR-BC\, is an artist and a registered and board certified Art Therapist. She is licensed as a Marriage and Family Therapist and Mental Health Counselor and is currently in private practice in Los Angeles\, California. Ms. Hayes developed the art therapy program at the Rhode Island School of Design–Continuing Education. For the past 15 years\, Ms. Hayes has worked in numerous psychiatric settings with a variety of clients. Currently\, her focus includes families\, couples\, adults and children struggling with mood and anxiety disorders\, addiction\, eating disorders\, abuse and grief-related issues. Ms. Hayes has an undergraduate degree in Fine Arts from Parsons School of Design in New York City and a graduate degree in Marriage and Family Therapy and Art Therapy from Notre Dame de Namur University in Belmont\, California. For more information about Ms. Hayes\, please visit her website at\: www.hayesarttherapy.com.
Disclaimer\:
This event qualifies for one CE credit. Only registered attendees will have access to CE. A Cross Country Education web account is required to attend. There is no charge for a CCE web account. It is recommended that you join the meeting 15 to 20 minutes early. Speaker phone sound quality is poor and it is recommended that they not be used to listen to the event.
Technical requirements\:
To view this webinar you will need to download the WebEx Application. You will be prompted to download it when you first enter the site. To save time\, you can setup prior to the meeting by following this link\: https\://apidemoeu.webex.com/apidemoeu/meetingcenter/mcsetup.php
Who Should Attend\:
Drug and Alcohol Abuse Counselors\, Pediatricians\, Physicians\, Art Therapists\, Pastoral Counselors\, Guidance Counselors\, Youth Pastors\, Youth Counselors\, Educators
KeellsSuper is a leading supermarket chain with 50-plus outlets in Sri Lanka\, and it offers the only online supermarket in the country.
In 2005\, JKH implemented SAP ERP across it’s 70 subsidiaries. With the recent decision to move KeellsSuper from the group ERP deployment to its own line of business (LOB) specific instance of SAP ERP\, arose the need for an integrated SAP/POS system.
JKH evaluated 3 key integration options -
Implement an in-house Custom RPC like integration solution to integrate with POS systems
Use SAP’S Own middleware
Use a 3rd party ESB based middleware solution.
Join Harsha Senanayake Head of Enterprise Solutions and Nalaka Umagiliya\, Head of IT Retail and Consumer Foods of John Keells Holding PLC along with Asanka Abeysinghe Director Solutions Architecture and Sumedha Rubasinghe\, Architect at WSO2 for a discussion on the implementation of SAP ERP in JKH. This session will commence with an introduction to the customer requirement followed by an in depth discussion of the WSO2 Solution and illustrate the benefits it posed in responding to the client requirement.
Asanka\, Director Solutions Architechure at WSO2\, manages solutions architects and technical consultants. He is also the technical owner of customer engagements and solutions. He counts over 10 years industry experience working on projects ranging from desktop and web applications through to high scalable distributed systems and service-oriented architectures in the financial domain\, mobile platforms and business integration solutions.
With over 10 years industry experience in Java\, J2EE and database technologies\, Sumedha is an Architect and Senior Manager at WSO2. He initiated the award winning WSO2 Data Services Server product and has also contributed heavily to WSO2′s Governance Registry\, Application Server\, BAM\, and Carbon platform products.
Harsha is the Head of Enterprise Solutions at John Keells Holding PLC\, a blue-chip conglomerate in Sri Lanka. He has over 10 years of industry experience working on projects ranging from Enterprise Architecture Planning and Business Case formulation\, complex Systems Integrations\, ERP presales and implementations to Software Development.
Nalaka Umagiliya is the Head of Business Systems for Consumer Foods and Retail Sectors of John Keells Holdings PLC. He specializes n IS/ IT strategy implementation using emerging technologies and ERP systems (SAP) and counts over 14 years of industry experience.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120216T150000Z DTEND;VALUE=DATE-TIME:20120216T150000Z UID:http://www.webinarcentral.net/content/ins-and-outs-ctms-data-migration URL;VALUE=URI:http://www.webinarcentral.net/content/ins-and-outs-ctms-data-migration SUMMARY:The Ins and Outs of CTMS Data Migration DESCRIPTION:You are considering implementing a new clinical trial management system (CTMS)\, or maybe you have already made the decision. But you are wondering\: What should we do with the data in our legacy system? Is it worth migrating? Should we migrate all of the data or just some of it? When should we migrate? What methods should we use?
Join BioPharm Systems' Param Singh\, vice president of clinical trial management solutions\, for this complimentary one-hour session that will\:
• Explore all facets of data migration
• Offer guidance applicable to any organization
• Include a live demonstration of ASCEND-Migrate\, a data migration tool designed to streamline the migration from any investigator database to Oracle’s Siebel Clinical application
Thursday\, February 16\, 2012 @\:
7\:00 a.m. Pacific Time
8\:00 a.m. Mountain Time
9\:00 a.m. Central Time
10\:00 a.m. Eastern Time
15\:00 UK Time
16\:00 Central European Time
This training will show how you can handle customer complaints in compliance with FDA and ISO Regulations. We will discuss the best ways to document customer feedback\, what constitutes a complaint\, what do with \\"non-complaint\\" feedback\, and how to include complaint trending into your firm’s CAPA program.
Why You Should Attend\:
Negative customer feedback about a medical device's performance or safety is a strong indicator of whether a firm's manufacturing process is in control. This feedback is therefore subject to many requirements in both the QSR and ISO 13485. Failure to follow up on complaints about medical devices is among the most frequently cited observations on FDA-483s. This session will include the requirements for defining\, documenting\, and implementing a complaint-handling system\, including the requirements for complaint review\, investigation\, and corrective action\, as well as the ISO-specific implications.
This complaint handling webinar session will discuss the best way to document customer feedback\, what constitutes a complaint\, and what do with \\"non-complaint\\" feedback. Also contained will be a suggested method on including complaint trending into your firm's CAPA program. Additionally\, the application of risk management to a complaint handling system will be reviewed\, and a specific risk management system explained.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120216T160000Z DTEND;VALUE=DATE-TIME:20120216T170000Z UID:http://www.webinarcentral.net/content/social-media-and-marketing-fda-regulated-products-webinar-complianceonline URL;VALUE=URI:http://www.webinarcentral.net/content/social-media-and-marketing-fda-regulated-products-webinar-complianceonline SUMMARY:Social Media and Marketing FDA Regulated Products - Webinar By ComplianceOnline DESCRIPTION:The webinar will discuss the do’s and don’ts for using social media in marketing FDA-regulated products. Common issues\, misconceptions\, perceptions\, and possible solutions will be discussed. The presentation will to familiarize you with the current FDA rules and help you plan for developments expected in the near future.
Why Should You Attend\:
The FDA recently held hearings addressing drug companies' use of social media and other online platforms to advertise. FDA also released a guidance document about manufacturers’ obligation regarding off-label information available about their products. Another guidance document about use of social media in marketing is expected soon. In addition\, FDA issued several letters to manufacturers indicating the rules for using social media.
But there is still much confusion among FDA regulated companies how to use social media for marketing effectively and still be compliant with regulations. How can medical device\, pharmaceutical and other FDA regulated industries use social media channels like Facebook\, Twitter\, YouTube and LinkedIn to get their message out in a way that is compliant with advertising and promotion regulations found in the Food Drug &\; Cosmetic Act? This 60-minute webinar will present ways to use social media that are compliant with FDA regulations. Practical regulatory strategies will be suggested to ensure compliance and balanced social media activity.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120216T150000Z DTEND;VALUE=DATE-TIME:20120216T154500Z UID:http://www.webinarcentral.net/content/iaq-i-%E2%80%93-introduction-indoor-air-pollutants-health-risks-solutions-0 URL;VALUE=URI:http://www.webinarcentral.net/content/iaq-i-%E2%80%93-introduction-indoor-air-pollutants-health-risks-solutions-0 SUMMARY:IAQ I – Introduction to Indoor Air Pollutants\, Health Risks & Solutions DESCRIPTION:Indoor air quality is easily compromised by a variety of factors.
Attend this webinar to find out more about indoor air pollutants such as
• Chemicals and VOCs
• Mold
• Smoke
• Bacteria and viruses
• Particles and dust
• Allergens and “asthmagens”
• And more
When trapped and re-circulated in a building\, these pollutants can accumulate and affect the health and well-being of building occupants.
The webinar will explore possible health effects of poor Indoor Air Quality\, simple steps to improve IAQ and an introduction to popular air filtration technologies as well as their benefits and shortcomings.
Reserve your seat for this free webinar and take control over the air you are breathing every day.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120216T160000Z DTEND;VALUE=DATE-TIME:20120216T170000Z UID:http://www.webinarcentral.net/content/conducting-reference-checks-background-checks-and-alcohol-and-drug-testing URL;VALUE=URI:http://www.webinarcentral.net/content/conducting-reference-checks-background-checks-and-alcohol-and-drug-testing SUMMARY:Conducting Reference Checks\, Background Checks\, and Alcohol and Drug Testing DESCRIPTION:This webinar will provide you tools and processes to verify a candidate’s qualifications in experience\, education\, character and work ethics. It will cover legal guidelines in doing reference and background checks.
Why Should You Attend\:
Hiring the right people is one of the most important decisions made in organizations today. When you are responsible for assuring the best hires\, it is essential for you to perform due diligence after the interview process and the favorite candidates are selected. Candidates may interview very well\, appear to be very competent\, and have an excellent history on paper\, but it is always important to verify that they are authentic. Some candidates who excel in interviewing skills can vastly exaggerate their competencies or past responsibilities and cover up any negative information about their past employment history.
The webinar will give you the tools and processes to help you get the information you need to verify a candidate’s qualifications in experience\, education\, character and work ethics as well as meeting any other requirements you have for the position. “Name\, rank\, and serial number” is not sufficient in discovering whether someone can do the job. We will cover what kinds of background checks are appropriate for different jobs and the best techniques to obtain the needed information as well as guidelines to follow in doing reference and background checks to assure being in compliance with employment law. We will also cover methods and policies on drug and alcohol testing.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120216T163000Z DTEND;VALUE=DATE-TIME:20120216T163000Z UID:http://www.webinarcentral.net/content/new-paradigm-product-training-merging-content-technology-service-free-live-webinar URL;VALUE=URI:http://www.webinarcentral.net/content/new-paradigm-product-training-merging-content-technology-service-free-live-webinar SUMMARY:A New Paradigm in Product Training - Merging Content\, Technology & Service - Free Live Webinar DESCRIPTION:We are all familiar with the traditional paradigm for product training - Instructor-led classroom training with fixed formats\, thick manuals distributed as reference materials\, rigid schedules\, limited or no community learning\, and with technology limited to merely providing access to training or information portals.
What makes this paradigm even more challenging is the lack of regular reinforcement of learning and the absence of any effort to market\, monitor and manage the training vision. Not surprisingly\, this traditional paradigm for product training can no longer support the evolving needs of current day employees who need anytime\, anywhere access to training and information\, in a format of their choice\, and with peer-to-peer interaction for collaborative learning.
Clearly\, a new paradigm in product training is required for any kind of training initiative to be a success today. Join us in this live webinar to find out what this new paradigm is all about and why it makes good business sense to adopt it. You will find answers to the following questions and more\:
What is the traditional paradigm for training? Why is it no longer relevant?
What is the new paradigm and what are the various components included in it?
What are the skills required to implement this new paradigm of training?
How can we seamlessly bring together the three components of content\, technology\, and service for delivering highly effective product training?
Discover why Inattentive ADHD is different from other types of ADHD and learn the latest information about screening\, SCT\, symptomatology\, comorbidities\, treatment modalities\, medication\, and how this disorder may be mentioned in DSM-5.
Full Description\:
Why is Inattentive ADHD Different? New Information
Attention-Deficit Hyperactivity Disorder\, Predominately Inattentive Type is NOT a “calmer” or “lighter” version of ADHD. The neurophysiology\, symptoms\, treatment methods\, and medications for this disorder are different than the other
types of ADHD. Since patients with Inattentive ADHD are not typically as disruptive as those with other types of ADHD\, this type is commonly misunderstood or goes unrealized by the mental health professional. Little research has been
done compared to Combined ADHD and most seminars and webinars only spend a small portion of time on Inattentive ADHD.
This one-hour course will provide participants with the latest information about screening\, Sluggish Cognitive Tempo (SCT)\, symptomatology\, comorbidities\, treatment modalities\, medication\, and how Inattentive ADHD may be mentioned in
DSM-5.
Course Includes\:
Live Q&\;A
Presentation Handout
Post session recording access
CE Credit
What You Will Learn\:
Identify the differences between Attention-Deficit/Hyperactivity Disorder\, Predominately Inattentive Type (Inattentive ADHD)\, and other forms of ADHD
Define treatment methods for Inattentive ADHD and how such methods are different than those for other forms of ADHD
Outline the common co-morbidities of Inattentive ADHD
Evaluate new research about Sluggish Cognitive Tempo and its relationship to ADHD
Discuss how Inattentive ADHD may be described in DSM-5
Your Presenter\:
KEVIN T. BLAKE\, PhD\, P.L.C.\, is a licensed psychologist and author with over 20 years of experience as a nationally recognized authority on learning disorders and ADHD in children\, adolescents\, and adults. This interest spurred from his
own struggles overcoming a reading disorder/dyslexia and hearing impairment.
Dr. Blake serves as a member of the American Psychological Association\, International Dyslexia Association\, Children and Adults with Attention Deficit Disorders\, Learning Disabilities Association\, and the National Attention Deficit
Disorder Association and was a 1991 delegate to the National Institute for Literacy’s “LEAD 2000 Congress\,” where he advised Congress on diagnostic and remediation issues.
Disclaimer\:
This event qualifies for one CE credit. Only registered attendees will have access to CE. A Cross Country Education web account is required to attend. There is no charge for a CCE web account. It is recommended that you join the meeting
15 to 20 minutes early. Speaker phone sound quality is poor and it is recommended that they not be used to listen to the event.
Technical requirements\:
To view this webinar you will need to download the WebEx Application. You will be prompted to download it when you first enter the site. To save time\, you can setup prior to the meeting by following this link\:
https\://apidemoeu.webex.com/apidemoeu/meetingcenter/mcsetup.php
Who Should Attend\:
Psychologists\, Social Workers\, Licensed Professional Counselors\, Marriage and Family Therapists\, School Psychologists\, Guidance Counselors\, Psychiatric Nurses\, Nurses\, Psychiatric Nurse Practitioners\, Case Managers\, Alcoholism and Drug
Abuse Counselors/Addiction Professionals\, Clergy\, School Administrators\, Physicians\, Psychiatrists\, Mental Health Administrators\, Special Education Teachers\, College Counselors
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120217T030000Z DTEND;VALUE=DATE-TIME:20120217T030000Z UID:http://www.webinarcentral.net/content/using-wso2-esb-sap-erp-retail-sector URL;VALUE=URI:http://www.webinarcentral.net/content/using-wso2-esb-sap-erp-retail-sector SUMMARY:Using the WSO2 ESB with SAP ERP in the Retail Sector DESCRIPTION:KeellsSuper is a leading supermarket chain with 50-plus outlets in Sri Lanka\, and it offers the only online supermarket in the country.
In 2005\, JKH implemented SAP ERP across it’s 70 subsidiaries. With the recent decision to move KeellsSuper from the group ERP deployment to its own line of business (LOB) specific instance of SAP ERP\, arose the need for an integrated SAP/POS system.
JKH evaluated 3 key integration options -
1. Implement an in-house Custom RPC like integration solution to integrate with POS systems
2. Use SAP’S Own middleware
3. Use a 3rd party ESB based middleware solution.
Join Harsha Senanayake Head of Enterprise Solutions and Nalaka Umagiliya\, Head of IT Retail and Consumer Foods of John Keells Holding PLC along with Asanka Abeysinghe Director Solutions Architecture and Sumedha Rubasinghe\, Architect at WSO2 for a discussion on the implementation of SAP ERP in JKH. This session will commence with an introduction to the customer requirement followed by an in depth discussion of the WSO2 Solution and illustrate the benefits it posed in responding to the client requirement.
Asanka\, Director Solutions Architechure at WSO2\, manages solutions architects and technical consultants. He is also the technical owner of customer engagements and solutions. He counts over 10 years industry experience working on projects ranging from desktop and web applications through to high scalable distributed systems and service-oriented architectures in the financial domain\, mobile platforms and business integration solutions.
With over 10 years industry experience in Java\, J2EE and database technologies\, Sumedha is an Architect and Senior Manager at WSO2. He initiated the award winning WSO2 Data Services Server product and has also contributed heavily to WSO2′s Governance Registry\, Application Server\, BAM\, and Carbon platform products.
Harsha is the Head of Enterprise Solutions at John Keells Holding PLC\, a blue-chip conglomerate in Sri Lanka. He has over 10 years of industry experience working on projects ranging from Enterprise Architecture Planning and Business Case formulation\, complex Systems Integrations\, ERP presales and implementations to Software Development.
Nalaka Umagiliya is the Head of Business Systems for Consumer Foods and Retail Sectors of John Keells Holdings PLC. He specializes n IS/ IT strategy implementation using emerging technologies and ERP systems (SAP) and counts over 14 years of industry experience.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120217T160000Z DTEND;VALUE=DATE-TIME:20120217T160000Z UID:http://www.webinarcentral.net/content/3-hr-virtual-seminar-osha-asbestos-and-mold-awareness-all-one-session URL;VALUE=URI:http://www.webinarcentral.net/content/3-hr-virtual-seminar-osha-asbestos-and-mold-awareness-all-one-session SUMMARY:3-hr Virtual Seminar - OSHA Asbestos and Mold Awareness\: All-in-One Session DESCRIPTION:This 3-hr virtual seminar - OSHA Asbestos and Mold Awareness - will cover OSHA's regulations on Asbestos and specific guidelines and general regulations on Mold.
Why Should You Attend\:
Asbestos is one of the most highly regulated substances\, and for good reasons as it’s a potent carcinogen with no known safe exposure. Of all of the toxic and hazardous substances it could have regulated\, OSHA chose to regulate Asbestos first.
Mold\, on the other hand\, is an even more ubiquitous contaminant in buildings\, yet OSHA has not even attempted any regulations specific to it. Instead\, they have a set of guidelines as well as several general regulations that all apply.
In this 3-hour session we will cover the required elements of the 2-hour awareness training OSHA requires for Asbestos\, as well as the OSHA Mold guidelines and many of their applicable regulations.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120217T160000Z DTEND;VALUE=DATE-TIME:20120217T190000Z UID:http://www.webinarcentral.net/content/3-hr-virtual-seminar-hipaa-privacy-and-security-audits-and-enforcement URL;VALUE=URI:http://www.webinarcentral.net/content/3-hr-virtual-seminar-hipaa-privacy-and-security-audits-and-enforcement SUMMARY:3-hr Virtual Seminar - HIPAA Privacy and Security Audits and Enforcement DESCRIPTION:This 3-hr virtual seminar on HIPAA Privacy and Security Audits and Enforcement will cover HIPAA Privacy\, Security\, and Breach Notification regulations (and the recent changes to them) and how they will be audited. Documentation requirements\, enforcement actions and how to prepare and respond to an audit will also be explored.
Why Should You Attend\:
The new HIPAA compliance audit program has been announced and is now under way\, bringing HIPAA compliance audits to up to 150 HIPAA Covered Entities by the end of 2012. If your organization is not ready\, the HIPAA rules have new\, significantly higher fines\, including mandatory minimum fines of $10\,000 for willful neglect of compliance.
In this session we will discuss the HIPAA audit and enforcement processes and how they apply to covered entities and business associates. We will explain the enforcement regulations and their recent changes. We will discuss what information and documentation needs to be prepared in advance so that you can be ready for an audit without notice. Sample information request forms and questions asked at prior audits will be presented. The session will also cover how to know if you may become the subject of an audit or enforcement action\, and what you can do to help limit your exposure. We will discuss how most enforcement actions come about and what can be done to prevent incidents that lead to enforcement.
The results of prior HHS audits (and their penalties) will be discussed\, including recent actions involving multi-million dollar fines and settlements. A plan for attaining compliance will be presented. The steps to follow to prepare for an audit and respond to an audit request will be outlined. In addition\, upcoming trends in information security risks will be discussed.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120221T180000Z DTEND;VALUE=DATE-TIME:20120221T180000Z UID:http://www.webinarcentral.net/content/dietary-supplement-regulatory-compliance-united-states-labeling-product-claims-updates-fda-w URL;VALUE=URI:http://www.webinarcentral.net/content/dietary-supplement-regulatory-compliance-united-states-labeling-product-claims-updates-fda-w SUMMARY:Dietary Supplement Regulatory Compliance in the United States\: Labeling\, Product Claims & Updates from the FDA - Webinar By GlobalCompliancePanel DESCRIPTION:This 90 minute live\, interactive webinar will review the dietary supplement regulations and discuss how to verify that your products are compliant\, while citing differences with food and drug regulations. We will also cover what qualifies a material as a dietary ingredient\, considerations for manufacturers and distributors\, requirements for compliant labeling and acceptable marketing claims. An update on FDA’s draft guidance for New Dietary Ingredients and an overview of the Dietary Supplement Labeling Act (both introduced in 2011) will also be discussed. At the conclusion of this 75 minute presentation\, there will be a 15 minute Q&\;A session with the speaker.
The FDA\, with assistance from the FTC\, has become increasingly aware of the large amount of dietary supplements that have come onto the market since the passage of the Dietary Supplement Health and Education Act in 1994. A growing public demand for supplements\, along with a relatively relaxed pre-market approval process\, has resulted in a flurry of companies creating and marketing their own dietary supplements in the United States. With FDA beginning to take a stronger stance on Dietary Supplement enforcement\, it is important for companies to verify that their products comply with the latest regulations and provisions.
Areas Covered In the Session\:
Dietary Supplement Overview
What is a dietary supplement?
Supplements vs. Pharmaceuticals/OTC Drugs/Conventional Foods
Regulatory Structure
FDA Structure regarding Dietary Supplements
Industry Groups
History of Dietary Supplement Regulation
Early History &\; DSHEA
Code of Federal Regulations
Manufacturing Considerations
Company &\; Facility Registration
GMP Requirements
Dietary Ingredients
What qualifies as a dietary ingredient?
Old dietary ingredients vs. New dietary ingredients
New Dietary Ingredient Notification (NDIN)
Updated New Dietary Ingredient Guidance from FDA
Labeling Considerations
Display Panels &\; Layout
Supplement Facts Panel Requirements
Labeling Claims
Health vs. Disease vs. Structure/Function claims
Disclaimers/Substantiation
Notification of labeling claims to FDA
Dietary Supplement Labeling Act
Advertising Considerations
FDA vs. FTC jurisdiction &\; enforcement
Expressed vs. Implied Claims
Disclosures &\; Claim Substantiation
Testimonials
Questions &\; Answers
Who will benefit\:
Executives of Dietary Supplement companies
Regulatory Compliance Professionals
Quality Assurance Professionals
Dietary Supplement Manufacturers
Dietary Supplement Distributors
Sales/Marketing Personnel
Price List\:
Live \: $245.00
Corporate live \: $995.00
Recorded \: $295.00
webinars@globalcompliancepanel.com
http\://www.globalcompliancepanel.com
Phone\: 800-447-9407
Fax\: 302-288-6884
1000 N West Street | Suite 1200 | Wilmington | DE | Zip 19801 | USA
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120221T160000Z DTEND;VALUE=DATE-TIME:20120221T173000Z UID:http://www.webinarcentral.net/content/design-history-files-device-master-records-device-history-records-and-technical-files-0 URL;VALUE=URI:http://www.webinarcentral.net/content/design-history-files-device-master-records-device-history-records-and-technical-files-0 SUMMARY:Design History Files\, Device Master Records\, Device History Records\, and Technical Files DESCRIPTION:Why Should You Attend\:
Global companies must meet different product design documentation for the U.S. and the European Union / Common Market. The cGMPs mandate Design Control and the Design History File (DHF). In order to sell globally\, the EU's CE-marking documentation is a requirement -- the Technical File or Design Dossier. Currently they serve different purposes\, support different goals\, but the TF/DD is moving in the direction of the DHF. And the DHF may soon borrow some features required in the TF/DD. Being aware of the similarities and differences can further concurrent development / documentation\, and/or updates to both. What are DMRs and DHRs relationship to DHFs\, TF/DDs?
This webinar will examine the existing and proposed requirements for the FDA's DHF and the MDD's TF/DD -- how to meet and document them. Their differing purposes / goals\, required and desirable contents and areas requiring frequent re-evaluation / update will be discussed. Similarities and differences\, and future convergences and trends will be examined. Typical DHF Table of Contents\, Technical File or Design Dossier Table of Contents will be presented.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120221T180000Z DTEND;VALUE=DATE-TIME:20120221T180000Z UID:http://www.webinarcentral.net/content/risk-assessment-compliance-using-easy-fill-out-documentation-webinar-globalcompliancepanel URL;VALUE=URI:http://www.webinarcentral.net/content/risk-assessment-compliance-using-easy-fill-out-documentation-webinar-globalcompliancepanel SUMMARY:Risk Assessment - Compliance Using Easy To Fill Out Documentation - Webinar By GlobalCompliancePanel DESCRIPTION:This webinar teaches how to determine and document risk in a process in order to reduce validation time and ensure compliance.
What makes this session unique are the real life examples that make application of the techniques understandable in the context of any validation project. It includes a workshop for participants to perform their own hazard analysis so they are proficient in applying the risk-based techniques.
Areas Covered in the Session\:
Interactive real life examples.
How to identify risk and establish mitigations.
How to use the hazard analysis to make validation efficient.
How to document the risk assessment using a template
How risk assessment reduces validation time.
Determine risk in a process to reduce the testing effort.
Traceability made automatic
Workshop exercises.
Who Will Benefit\:
IT
QA
QC
Laboratory staff
Managers
GMP\, GCP\, GLP professionals
Price List\:
Live \: $245.00
Corporate live \: $995.00
Recorded \: $295.00
webinars@globalcompliancepanel.com
http\://www.globalcompliancepanel.com
Phone\: 800-447-9407
Fax\: 302-288-6884
1000 N West Street | Suite 1200 | Wilmington | DE | Zip 19801 | USA
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120221T190000Z DTEND;VALUE=DATE-TIME:20120221T190000Z UID:http://www.webinarcentral.net/content/suicide-loss-what-all-medical-professionals-should-know-0 URL;VALUE=URI:http://www.webinarcentral.net/content/suicide-loss-what-all-medical-professionals-should-know-0 SUMMARY:Suicide Loss\: What All Medical Professionals Should Know DESCRIPTION:Led by an experienced therapist in the field\, this webinar outlines the complex issues faced by survivors of suicide and provides medical and behavioral health professionals with treatment strategies for individuals at all stages of
recovery.
Full Description\:
Every 15 minutes someone in the United States dies by suicide\, leaving behind 6-8 loved ones\, known as survivors of suicide. The word suicide continues to be associated with shame and stigma\, leaving many individuals who need mental
health treatment and those left behind by suicide afraid to reach out for help. Many survivors hold a lot of their feelings and thoughts inside\, even while seeking treatment.
The complexity of suicide and suicide loss leave many professionals feeling under-educated and ill-prepared to work with a survivor in treatment. Led by an experienced therapist and specialist in the field\, this webinar is designed to
investigate the complex grieving process associated with this loss and to provide new strategies for working with individuals at all stages of recovery. Ms. Falasco brings both her extensive training in prevention and postvention to this
webinar\, as well as her personal experiences as a suicide survivor.
Course Includes\:
Live Q&\;A
Presentation Handout
Post session recording access
CE Credit
What You Will Learn\:
Identify the effects of suicide loss on survivors and helpers
Examine the current statistics on suicide and the nature of suicide
Identify grief reactions\, grieving styles\, and symptoms of traumatic grief
Describe the nature\, process\, and phases of suicide loss
Describe suicide postvention measures and loss support resources available to survivors
Learn specific interventions and techniques to assist the survivor through the mourning process
Your Presenter\:
Linda Falasco\, LCSW\, a licensed clinical social worker with over 20 years of experience. Ms. Falasco is a graduate of Temple University with a Masters in Social Work and has extensive post-masters training in child development\, play
therapy\, and bereavement. A seasoned lecturer on suicide loss\, Ms. Falasco brings both her extensive training in prevention and postvention to this webinar\, as well as her personal experiences as a suicide survivor.
Disclaimer\:
This event qualifies for one CE credit. Only registered attendees will have access to CE. A Cross Country Education web account is required to attend. There is no charge for a CCE web account. It is recommended that you join the meeting
15 to 20 minutes early. Speaker phone sound quality is poor and it is recommended that they not be used to listen to the event.
Technical requirements\:
To view this webinar you will need to download the WebEx Application. You will be prompted to download it when you first enter the site. To save time\, you can setup prior to the meeting by following this link\:
https\://apidemoeu.webex.com/apidemoeu/meetingcenter/mcsetup.php
Who Should Attend\:
Clergy\, Counselors\, Drug and Alcohol Counselors\, Educators\, Hospital (Clinical)\, Long-Term Care (Clinical)\, Marriage and Family Therapists\, Nurse Practitioners\, Psychologists\, Social Workers
Indoor Air Quality Challenges at the Office
A healthy workplace starts with healthy air
A majority of workers spend 40 or more hours at the office – and poor indoor air quality can affect their performance\, productivity and well-being\, which in turn can hurt a company’s bottom line.
In this webinar\, we explore common aspects of IAQ and offer an in-depth analysis relating to air quality and the need for proper indoor air management to avoid health hazards and related complications.
Find out what you can do to improve the indoor air quality in your workplace\, what questions to ask and how a healthier work environment can benefit the employees as well as the company.
We will propose an effective\, preventive IAQ management program that addresses many areas\, including source control – ventilation – humidity control – filtration.
Join us in Part II of our Webinar Series on IAQ Management at the workplace!
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120222T150000Z DTEND;VALUE=DATE-TIME:20120223T230000Z UID:http://www.webinarcentral.net/content/z%E2%80%99s-microbial-control-monitoring-and-validation-pharmaceutical-water-systems URL;VALUE=URI:http://www.webinarcentral.net/content/z%E2%80%99s-microbial-control-monitoring-and-validation-pharmaceutical-water-systems SUMMARY:The A to Z’s of Microbial Control\, Monitoring and validation of Pharmaceutical Water Systems DESCRIPTION:Course Description\:
All pharmaceutical\, biologics\, and medical device facilities are likely to have high purity water systems. In spite of this purity\, microorganisms can flourish within these systems and lead to undesirable contamination of facility processes and their products. Of all the individuals at the facility who should understand the microorganisms in water systems and how best to monitor and control and them\, it should be the site’s microbiologists. Sadly\, this is often not the case due to the lack of familiarity with biofilm and its impact on water system sampling\, testing\, sanitization\, and routine maintenance.
This course is designed to provide a microbiology-focused education about all aspects of water systems and how biofilm manages to thrive there. Prior microbiological education or training\, though a plus\, is not a requirement. The instructor can provide the necessary background needed to understand this very important subject matter. This understanding is essential to the proper design\, validation\, operation\, monitoring\, and maintenance of a high purity water system. Without this understanding\, water system control consists of a set of rules that often don’t work and can cause very costly system downtime or even product recalls.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120222T180000Z DTEND;VALUE=DATE-TIME:20120222T180000Z UID:http://www.webinarcentral.net/content/reusable-device-cleaning-disinfection-and-sterilization-validations-overview-and-key-design- URL;VALUE=URI:http://www.webinarcentral.net/content/reusable-device-cleaning-disinfection-and-sterilization-validations-overview-and-key-design- SUMMARY:Reusable Device Cleaning\, Disinfection\, and Sterilization Validations\: Overview and Key Design Considerations for Device Engineers - Webinar By GlobalCompliancePanel DESCRIPTION:Validation of reusable medical devices requires that the manufacturer develop methods for cleaning (after use) washing to remove all foreign matter possibly disinfecting and repackaging for the next use.
The diversity of medical devices their intended use and classification in accordance with the food and drug administration requires that the manufacturer develop and validate the reprocessing of the medical device.
Reprocessing usually entails that the manufacturers thoroughly understand the design of the device and what potential hazards can occur if the device is not properly cleaned before reprocessing. This usually means that the manufacturer must establish clear and efficacious instructions on how to reprocess the medical device before reuse.
Why you should attend\: To assist you in the identification of key factors during the development of your protocol. you will be guided on how to identify key factors in the protocol design process. Key factors such as selection of chemical agents specifically biocidal agents and or biostatic agent(s). Identify testing that will be required to evaluate these proposed agents
Biocompatibility issues\, such as should you test for cytotoxicity\, tolerable contact limit (TCL) as stated in ISO 10993-7.
If you require sterilization of your reusable should packaging and penetration issues be addressed. What will be the required sterility specifications for your product. Sterility assurance issues will be discussed.
You will be able to write and review medical device reprocessing protocols and assists in the revision process\, in order to eliminate or minimize process interruptions.
Areas Covered In the Session\:
Key points regarding protocol development
A summary of standards
Key tests to be familiar with
Expected results
Packaging issues
Labeling issues
Who will benefit\:
Engineering
Quality
Validation
Microbiology
Process/ Scientist
Manufacturing
Regulatory Affairs
Price List\:
Live \: $245.00
Corporate live \: $995.00
Recorded \: $295.00
webinars@globalcompliancepanel.com
http\://www.globalcompliancepanel.com
Phone\: 800-447-9407
Fax\: 302-288-6884
1000 N West Street | Suite 1200 | Wilmington | DE | Zip 19801 | USA
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120222T180000Z DTEND;VALUE=DATE-TIME:20120222T180000Z UID:http://www.webinarcentral.net/content/implement-tougher-supplier-audit-program-webinar-globalcompliancepanel URL;VALUE=URI:http://www.webinarcentral.net/content/implement-tougher-supplier-audit-program-webinar-globalcompliancepanel SUMMARY:Implement a Tougher Supplier Audit Program - Webinar By GlobalCompliancePanel DESCRIPTION:There is a pervasive public perception that the FDA has been ineffective in protecting the public. Recent news events seem to support this perception. The FDA is working hard to change that perception. Industry must be prepared to adapt\, and recognize that such adaptation will actually work to their long-term benefit.
This webinar will discuss and evaluate the effects that this call for change has on a company and its selection\, audit\, use and on-going relations with its suppliers of services and products / components. What are the \\"new\\" expectations for the COA and COC? How can companies address the FDA's stated desire to require \\"on-site\\" audit of all Pharma suppliers? Expectations for meaningful\, results driven actions that addresses and resolve any underlying compliance issues or product problems are increasing among regulatory agencies worldwide. To meet the new regulatory climate and be competitive\, companies need to reevaluate their vendors and the methods used in selecting\, evaluating\, auditing\, retaining or cutting adrift such regulatory \\"partners\\".
Why you should attend\: The last few years have seen the U.S. FDA come under increasing negative public scrutiny. High profile drug recalls\, food chain problems and contamination\, import problems\, resignations. The commissioner vows no more \\"business as usual\\". Data in cGMP records must be more science based. Companies are outsourcing more\; with some thinking they can also outsource some of their cGMP compliance as well. Thus\, the FDA has indicated that a key area they are focusing attention is on a company's suppliers\, for both services and products / components. Why needed? FDA expectations? How are successful companies meeting this challenge. Tools that need to be put in place or enhanced. The required supporting infrastructure for COAs and COCs. Meeting the challenges of more \\"on site\\" audits. Getting supplier buy-in. Coping with \\"rogue\\" suppliers.
Areas Covered in the Session\:
Regulatory supplier \\"Hot Buttons\\"
Classify suppliers\; Supplier requirements by \\"classification\\"
What's behind the COA? The COC?
The FDA's increasing emphasis on the site audit
Types of remote audits
Entropy\, and maintaining the relationship
Who Will Benefit\:
Senior management in Drugs\, Devices\, Biologics\, Dietary Supplements
QA
RA
R&\;D
Engineering
Production
Operations
Consultants
Price List\:
Live \: $245.00
Corporate live \: $995.00
Recorded \: $295.00
webinars@globalcompliancepanel.com
http\://www.globalcompliancepanel.com
Phone\: 800-447-9407
Fax\: 302-288-6884
1000 N West Street | Suite 1200 | Wilmington | DE | Zip 19801 | USA
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120222T160000Z DTEND;VALUE=DATE-TIME:20120222T160000Z UID:http://www.webinarcentral.net/content/banish-poor-application-performance-eliminate-business-disruptions-increase-end-user-product URL;VALUE=URI:http://www.webinarcentral.net/content/banish-poor-application-performance-eliminate-business-disruptions-increase-end-user-product SUMMARY:Banish Poor Application Performance\: Eliminate Business Disruptions\, Increase End User Productivity DESCRIPTION:Live 30-Minute Webinar\, Bonus VDI Whitepaper
Are you ready to gain the proactive ability to rapidly respond to end user problems (before they call the help desk)? Then you won’t want to miss a special event that will show you the latest innovation in end user monitoring. Register today for a 30-minute webinar hosted by Aternity – the company that redefines real end user experience management. Aternity will showcase its latest release – Version 5.0 of its Frontline Performance Intelligence (FPI) Platform – during the webinar.
About this 30-Minute Webinar
Join Aternity for a live 30-minute webinar and see how Aternity’s Frontline Performance Intelligence (FPI) Platform v5.0 uniquely monitors the three primary components that dynamically interact at all times to define and impact an end user’s experience as an IT consumer\: Application Performance\, Device Performance\, and User Productivity. Frontline Performance Intelligence is the result of the real-time aggregation\, analysis and correlation of all these metrics\, ultimately closing the visibility gap from the Desktop Vantage Point.
As a special bonus\, all webinar registrants will receive a copy of Aternity's newest whitepaper on Monitoring End User Experience in VDI Environments.
Join Us
Select which session you would like to join!
11 AM ET / 8 AM PT\: Register Now!
1 PM ET / 10 AM PT\: Register Now!
What Attendees Will Learn
Attendees will see a live demonstration of the Aternity FPI Platform v5.0 and learn about the latest innovative capabilities for closing the visibility gap and driving winning performance including\:
• Web 2.0\, .Net\, Java\, Thick Client\, VDI\, Citrix and Enterprise Outlook Monitoring
• How Frontline Performance Intelligence delivers fast Mean-Time-To-Repair (MTTR) for the toughest desktop application problems
• Advanced analytics that drives rapid response to performance issues
• Privacy Compliance and Massive Scalability for Ensuring Enterprise Readiness of your Application Performance Management (APM) strategic initiatives
Who Should Attend
• IT Operations Leaders
• Application Owners
• Desktop Engineers
• Help Desk Personnel • Application Architects
• Performance Engineers
• ITOs\, ISVs\, SaaS Providers\, SIs and LARs
Featured Speaker
Trevor Matz ~ President and CEO\, ATERNITY
Trevor Matz is the President and CEO of Aternity. Matz leads Aternity as the company scales to redefine end user experience management by providing the industry’s first frontline intelligence platform. Matz has built and led world class sales and marketing organizations for enterprise software and services companies globally. Prior to joining Aternity\, Matz served as worldwide managing director of Application Integration for InterSystems Corporation where he took Ensemble from launch through recognition as the #1 Integration Platform in HealthCare.
This Japan Regulatory and Clinical Trial Requirements training will cover Japan Regulatory Agency Structure and Responsibilities\, its review process for decision-making and approval\, requirements for clinical trials in Japan and the procedures for conducting clinical studies in the country and reporting them.
Why Should You Attend\:
This 6 hour virtual seminar will help you gain a comprehensive understanding of the Regulatory Structure\, Clinical Trial Requirements and the Conduct of Running Clinical Research in Japan. It will prepare you for the regulatory approval processes\, Agency meetings\, the complexities of running studies in Japan\, the importance of partner selection and add the cultural knowledge needed for success. The recent changes made by PMDA to be more sponsor-friendly will be reviewed. Real world experiences on actual interactions with the Agency since these changes\, will also be discussed.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120223T150000Z DTEND;VALUE=DATE-TIME:20120224T230000Z UID:http://www.webinarcentral.net/content/auditing-and-administrating-human-resource-policies-and-practices URL;VALUE=URI:http://www.webinarcentral.net/content/auditing-and-administrating-human-resource-policies-and-practices SUMMARY:Auditing and Administrating Human Resource Policies and Practices DESCRIPTION:Course Description\:
This two-day seminar provides information and techniques for handling human resources practices legally and effectively. Beginning with an overall audit of human resources practices\, this seminar covers legal requirements\, employment policies\, employee record maintenance\, employment practices\, performance management\, discipline and terminations. Each section will give proactive measures and best practices to assure the organization has equitable and effective human resource management.
Who Will Benefit\:
- Vice Presidents\, Directors\, &\; Managers of Human Resources
- Employment Managers\, Chief Talent Officers\, Recruiters
- Employee Relations Professionals
- HR Coordinators/Supervisors/Administrators
- HR Analysts
- Supervisors
- Auditors
This 90-minute training will provide an introduction to FDA’s rules governing pet food product development and formulation\, manufacturing\, labeling\; and marketing and promotion. In addition to facility inspections and product recalls\, the webinar will summarize and assess FDA’s enforcement activity in the U.S. pet food market paying particular attention to enforcement trends and risks.
Why Should You Attend\:
This webinar focuses on FDA rules governing the development\, formulation (including ingredients and food additives)\, manufacture\, testing\, labeling\; and marketing and promotion of pet food in the U.S. It will include a comprehensive overview of the pet food label\; FDA’s rules governing the use of labeling and promotional claims\; facility inspections\, product recalls\; and FDA enforcement action.
Paying particular attention to the FDA’s recognition of new foods and ingredients\, the webinar will also focus on the FDA’s regulation of food and food additives including the pre-marketing clearance requirement\, the food additive petition process and the process for showing that an ingredient is Generally Recognized as Safe (“GRAS”). An introduction to the function and responsibilities of the Association of American Feed Control Officials (AAFCO) will also be provided.
FDA’s regulation of products marketed as veterinary dietary supplements or nutraceuticals will also be discussed including the use of health claims in conjunction with the promotion and sale of such products in the U.S. A summary of the FDA’s past enforcement activities including the 2007 melamine incident and an introduction to the animal drug approval process will also be provided.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120223T160000Z DTEND;VALUE=DATE-TIME:20120223T170000Z UID:http://www.webinarcentral.net/content/accelerating-bioassay-transfer-gmp-environment-webinar-complianceonline URL;VALUE=URI:http://www.webinarcentral.net/content/accelerating-bioassay-transfer-gmp-environment-webinar-complianceonline SUMMARY:Accelerating Bioassay Transfer in a GMP Environment - Webinar By ComplianceOnline DESCRIPTION:This Bioassays webinar will systematically outline the steps needed to successfully transfer validated biological assays between GMP/GLP labs and also acquire non-validated assays for GMP/GLP development.
Why Should You Attend\:
50% of the drugs presently in discovery are biopharmaceuticals - these numbers lead to an \\"outsource or perish\\" philosophy for GMP/GLP development\, validation and sample analysis. Unlike synthetic drugs requiring only straightforward analytical testing biopharmaceuticals require more elaborate assays to attain regulatory compliance. The industry has a significant underestimation of the discipline\; skills and planning required to successfully transferring these assays. Naiveté in this area causes loss of precious time and money during development.
Participants in this seminar will attain a valuable checklist of critical information that will reduce delay and confusion during method transfer. The hands-on\, common sense approach will provide a chronological pathway that can easily be adapted for any complex assay.
Areas Covered in the seminar\:
This webinar systematically outlines the steps needed to successfully transfer validated biological assays between GMP/GLP labs and also acquire non-validated assays for GMP/GLP development. Topics to be addressed are\:
- Setting a realistic timeline for your assay transfer.
- Issues that need to be addressed in preliminary discussions between the labs.
- Proper method writing.
In this sterility assurance documentation webinar\, you will learn specifically what information is required in sterility assurance documentation for injectable drug products and how to present it in CTD format. You will understand differences in content for terminal sterilization versus aseptic processes.
Why Should You Attend\:
Having a plan for gathering and compiling appropriate sterility assurance documentation to be included in a global marketing application is essential for injectable drug products. In this session we will provide an overview of current regulatory guidance and compendial requirements associated with sterilization validation and control of microbial quality. We will review what information is needed\, what level of detail is included\, and how to present the documentation in CTD format.
Attendees will also learn what data and information need to be included in your submission for different approaches (terminal sterilization vs. aseptic processes) to manufacturing a sterile drug product. We will review information needed in support of the sterilization and depyrogenation of container closure components\, filter validation\, heat penetration and distribution studies\, and container closure integrity testing.
In addition the speaker will also focus on the need for periodic requalification of sterile processes and review requirements for use of parametric release in lieu of sterility testing for batch release\, which substantially shortens the release timeline.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120223T160000Z DTEND;VALUE=DATE-TIME:20120223T170000Z UID:http://www.webinarcentral.net/content/understanding-design-controls-medical-devices-webinar-complianceonline URL;VALUE=URI:http://www.webinarcentral.net/content/understanding-design-controls-medical-devices-webinar-complianceonline SUMMARY:Understanding Design Controls for Medical Devices - Webinar By ComplianceOnline DESCRIPTION:This webinar will cover the basics of design controls for medical devices\, and provide recommendations for implementation of a compliant design control system. Also discussed will be design control requirements for devices already in distribution. Documentation requirements for each design stage will be included as well.
Why You Should Attend\:
Prior to introduction of a new device\, or even a modified design for an existing device\, a systematic process must be followed. This process must ensure that all requirements are met. A firm's design control process must meet all regulatory requirements\, but at the same time not be as unwieldy as the present a barrier to timely market introduction. This webinar will cover the basics of design controls\, and provide recommendations for implementation of a compliant design control system. Also discussed will be design control requirements for devices already in distribution. Documentation requirements for each design stage will be included as well.
Areas Covered in the seminar\:
- History of design control.
- Design planning.
- Design input/output.
- Design reviews.
- Design documentation.
- Design transfer.
Free Tech Webinar\:
ENTERPRISE MOBILITY WITH SAP
Presented by Vikrant Raj
Thursday\, February 23\, 2012 - 01\:00 PM – 2\:00 PM EST
Corp-Corp.com cordially invite you to join a Technology related webinar on title “ENTERPRISE MOBILITY WITH SAP\\".
Webinar Highlights
Value of Mobile Solutions to the Enterprise.
SAP Going Mobile.
Mobile Apps Development Tools in SAP World.
Strategy for Enterprise Mobility.
Speaker's Profile\:
Vikrant Raj\, a SAP Netweaver Java/Portal professional\, is having extensive experience of SAP Consulting for Configuration and implementation of SAP Netweaver Portal\, Designing &\; Developing enterprise scale composite applications using the key NetWeaver components (CE/BPM\, BRM\, CAF–Core &\; GP\, WebDynpro Java) and Sybase Unwired Platform for Mobile Apps. He has enormous international experience and has led a SAP Business ByD product development team in past.
Registration\:
To register for this webinar\, Visit http\://www.corp-corp.com/blog/enterprise-mobility-with-sap/?aid=ccwrc
There will be an opportunity to ask your questions and doubts at the end of the webinar. Register now and join with us. Feel free to forward this message to your friends and colleagues.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120223T180000Z DTEND;VALUE=DATE-TIME:20120223T184500Z UID:http://www.webinarcentral.net/content/iaq-i-%E2%80%93-introduction-indoor-air-pollutants-health-risks-solutions URL;VALUE=URI:http://www.webinarcentral.net/content/iaq-i-%E2%80%93-introduction-indoor-air-pollutants-health-risks-solutions SUMMARY:IAQ I – Introduction to Indoor Air Pollutants\, Health Risks & Solutions DESCRIPTION:Indoor air quality is easily compromised by a variety of factors.
Attend this webinar to find out more about indoor air pollutants such as
• Chemicals and VOCs
• Mold
• Smoke
• Bacteria and viruses
• Particles and dust
• Allergens and “asthmagens”
• And more
When trapped and re-circulated in a building\, these pollutants can accumulate and affect the health and well-being of building occupants.
The webinar will explore possible health effects of poor Indoor Air Quality\, simple steps to improve IAQ and an introduction to popular air filtration technologies as well as their benefits and shortcomings.
Reserve your seat for this free webinar and take control over the air you are breathing every day.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120223T230000Z DTEND;VALUE=DATE-TIME:20120223T230000Z UID:http://www.webinarcentral.net/content/bullying-what-every-educator-should-know-and-do URL;VALUE=URI:http://www.webinarcentral.net/content/bullying-what-every-educator-should-know-and-do SUMMARY:Bullying\: What Every Educator Should Know and Do DESCRIPTION:Drexel University Online is offering a free webinar that offers tips and advice educators can use to be proactive about bullying. The event will be held online February 23\, 2012. To sign for the event\, please visit http\://www.drexel.com/openhouse/viewevent.aspx?e=13174
About Drexel
Drexel University Online offers a convenient way to earn a reputable\, accredited degree online. Drexel's online degree programs include but are not limited to online engineering\, online nursing\, and online engineering programs.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120224T130000Z DTEND;VALUE=DATE-TIME:20120224T190000Z UID:http://www.webinarcentral.net/content/full-day-virtual-seminar-validation-analytical-procedures-use-pharmaceutical-industry URL;VALUE=URI:http://www.webinarcentral.net/content/full-day-virtual-seminar-validation-analytical-procedures-use-pharmaceutical-industry SUMMARY:Full-day Virtual Seminar\: Validation of Analytical Procedures for Use in the Pharmaceutical Industry DESCRIPTION:This 6-hr virtual seminar will review analytical procedures used in assessing quality\, safety and efficacy of drug products. It will cover the ICH and USP guidelines for procedure validation and help you ensure robust validation of analytical procedures for drug substances and products.
Why Should You Attend\:
This 6-hr training will examine the analytical tools used throughout a drug product life cycle. There is a broad range of assays and techniques used to measure the quality\, safety and efficacy of a drug substance or a drug product. The training will challenge attendees to give thoughtful evaluation of their current strategies or to develop strategies from the ground up. The CFR regulations and guidance from the USP and ICH will be used as references and in support of creating a sound approach to the validation of analytical procedures for drug substances and products.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120224T160000Z DTEND;VALUE=DATE-TIME:20120224T173000Z UID:http://www.webinarcentral.net/content/avoiding-discrimination-when-recruiting-social-media-tools-webinar-complianceonline URL;VALUE=URI:http://www.webinarcentral.net/content/avoiding-discrimination-when-recruiting-social-media-tools-webinar-complianceonline SUMMARY:Avoiding Discrimination When Recruiting With Social Media Tools - Webinar By ComplianceOnline DESCRIPTION:This 90-minute training on Online Recruiting will provide a comprehensive review of how to avoid intentional and unintentional discrimination when using social media tools for recruiting.
Why Should You Attend\:
There is a wealth of personal information available in a social media profile. Much of this information is the same kind of information that would be requested on a traditional job application. But social media profiles often contain information about protected class status\; gender\, race and age may be inferred from photographs\, dates of birth may be displayed\, and information about family members\, relationship status and religious beliefs may be present. Having access to this kind of information can create the potential for intentional discrimination.
Additionally\, relying exclusively on social media for recruiting may lead to unintentional discrimination. There are significant differences in the demographic characteristics of the typical social media user and the typical individual in the civilian labor force. These demographic differences can lead to certain groups being excluded from the recruiting process\, thereby creating unintentional discrimination.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120224T160000Z DTEND;VALUE=DATE-TIME:20120224T170000Z UID:http://www.webinarcentral.net/content/leaping-lab-everything-about-waived-testing-webinar-complianceonline-1 URL;VALUE=URI:http://www.webinarcentral.net/content/leaping-lab-everything-about-waived-testing-webinar-complianceonline-1 SUMMARY:Leaping into Lab\: Everything about Waived Testing - Webinar By ComplianceOnline DESCRIPTION:This CLIA Webinar training will feature an in-depth look at CLIA Waived Testing. It will present the rules and regulations as well as the pros and cons of testing using Waived methods.
Why Should You Attend\:
Waived testing is an exciting way to leap into the world of laboratory testing. With over a hundred tests to choose from\, every speciality can find testing that will benefit the patients. We will explore the process to become a Waived lab and the many benefits of doing so. We will look at the rules and regulations set forth by CLIA under CMS and how to best meet them. We also will explore the many tests available and how they can benefit your patients. Waived labs make up the majority of laboratory testing taking place in this country and more tests are being added to the Waived category all the time. With less regulatory oversight\, ease of use and great re-imbursement\, Waived testing is hard to beat. We will also look at the future of Waived testing and where it is headed.
Areas Covered in the seminar\:
- Waived testing history and origins.
- Waived testing CLIA rules and regulations.
- Waived tests available and how they fit into your practice.
- How to apply for Waived testing and the State's role.
- The future of Waived testing and how it affects you
- Waived testing pitfalls to avoid.
This HR Audit training will help you assess your organization's risks and discusses the use of HR audits as a continuous audit process that strengths internal controls\, provides assurance of compliance\, and evaluates outcomes.
Why Should You Attend\:
The threats and risks from human resource management non-compliance are increasing. No longer measured in only fines\, penalties\, and awards\, non-compliance affects keys business metrics\, including the organization’s valuation\, credit rating and supply chain\, can significantly reduce managerial prerogatives\, and seriously damage the organization’s reputation and employment brand. As a result\, HR audits are evolving from an ad hoc audit activity to a critical element of organizations’ risk management and compliance processes.
This webinar assesses these risks and discusses the use of HR audits as a continuous audit process that strengths internal controls\, provides assurance of compliance\, and evaluates outcomes.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120224T160000Z DTEND;VALUE=DATE-TIME:20120224T173000Z UID:http://www.webinarcentral.net/content/international-trade-finance-payment-methods-webinar-complianceonline URL;VALUE=URI:http://www.webinarcentral.net/content/international-trade-finance-payment-methods-webinar-complianceonline SUMMARY:International Trade Finance Payment Methods - Webinar By ComplianceOnline DESCRIPTION:This 90-minute will help exporters and importers understand the three international trade finance methods of payment\; to include Letters of Credit\, Documentary Collections and Open Account\; and their variations. You will also learn the pros and cons of each method and what documents are used to effect each type.
Description
Companies that export and import products can use Documentary Letters of Credit\, Documentary Collections or Open Accounts to purchase and sell goods globally. Understanding the proper application and documents involved will assist in the reliable payment for goods sold. Understanding the proper application of each type of payment will provide the most competitive possible terms of sale.
This 90-minute webinar will help exporters and importers comprehensively understand the three international trade finance methods of payment and their variations. We will also review the pros and cons of each method and what documents are used to effect each type.
Learning objectives\:
Attendees will learn how to use and apply all three international trade finance payment methods and what documents are used to effect each type.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120224T180000Z DTEND;VALUE=DATE-TIME:20120224T180000Z UID:http://www.webinarcentral.net/content/art-therapy-interpreting-art-and-facilitating-communication-0 URL;VALUE=URI:http://www.webinarcentral.net/content/art-therapy-interpreting-art-and-facilitating-communication-0 SUMMARY:Art Therapy\: Interpreting the Art and Facilitating Communication DESCRIPTION:This one-hour webinar is designed to educate participants on how to guide clients through the process of describing their art work in order to understand patterns of behavior and ways to self-soothe.
Full Description\:
Evoke insight and understanding for your clients through their art work!
This webinar is designed to educate participants on how to ask open-ended questions to facilitate communication after clients have created the art work. Precise questions to be asked of the client will be provided based on specific art techniques. Participants will be discouraged from imposing their own interpretations on their clients' art work and will be guided on how to get clients to open up when describing their art-making experiences. This webinar will also provide specific techniques as well as the language needed to describe the directives. In addition\, you will learn what questions to ask that will best evoke insight and understanding from the client regarding unconscious motivations\, patterns of behavior\, and ways to self-soothe.
Course Includes\:
Live Q&\;A
Presentation Handout
Post session recording access
CE Credit
What You Will Learn\:
Discover an alternative method of communicating with clients
Examine effective Art Therapy techniques and learn how to implement them in session
Recognize the therapeutic power that art provides\, and how to affectively use the art as a means of communication
Identify skills for assessing and treating a multitude of clients
Discuss various art tasks and experience the healing process to promote coping skills in life
Your Presenter\:
PAMELA M. HAYES\, MFT\, LMHC\, ATR-BC\, is an artist and a registered and board certified Art Therapist. She is licensed as a Marriage and Family Therapist and Mental Health Counselor and is currently in private practice in Los Angeles\, California. Ms. Hayes developed the art therapy program at the Rhode Island School of Design–Continuing Education. For the past 15 years\, Ms. Hayes has worked in numerous psychiatric settings with a variety of clients. Currently\, her focus includes families\, couples\, adults and children struggling with mood and anxiety disorders\, addiction\, eating disorders\, abuse and grief-related issues. Ms. Hayes has an undergraduate degree in Fine Arts from Parsons School of Design in New York City and a graduate degree in Marriage and Family Therapy and Art Therapy from Notre Dame de Namur University in Belmont\, California. For more information about Ms. Hayes\, please visit her website at\: www.hayesarttherapy.com.
Disclaimer\:
This event qualifies for one CE credit. Only registered attendees will have access to CE. A Cross Country Education web account is required to attend. There is no charge for a CCE web account. It is recommended that you join the meeting 15 to 20 minutes early. Speaker phone sound quality is poor and it is recommended that they not be used to listen to the event.
Technical requirements\:
To view this webinar you will need to download the WebEx Application. You will be prompted to download it when you first enter the site. To save time\, you can setup prior to the meeting by following this link\: https\://apidemoeu.webex.com/apidemoeu/meetingcenter/mcsetup.php
Who Should Attend\:
Drug and Alcohol Abuse Counselors\, Pediatricians\, Physicians\, Art Therapists\, Pastoral Counselors\, Guidance Counselors\, Youth Pastors\, Youth Counselors\, Educators
Oppositional Defiant Disorder doesn’t have to be complicated! This web course provides mental health professionals with a three-step approach to treating the signs and symptoms of ODD and co-occurring disorders in children and teens\,
ages 4-14.
Full Description\:
Confronting Defiance
According to the AACAP\, evidence suggests that between 1 and 16% of children and adolescents have Oppositional Defiant Disorder (ODD). Challenged by basic rules of society\, this disorder causes a struggle between the parent and child and
ultimately the therapist and child. Tantrums\, arguing\, defiance\, blaming\, and anger when left untreated may disrupt classrooms\, strain families\, and lead to a risk of juvenile delinquency. Conflict may also go on to affect the
behavioral\, academic\, and social success of the child.
This webinar discusses ODD\, similar disorders\, and the effect on young children and teens. Using a three-step approach to intervention called SimpleThree\, mental health professionals will learn how to treat ODD symptoms in children and
adolescents as well as educate parents to reinforce good behavior to maintain success.
Course Includes\:
Live Q&\;A
Presentation Handout
Post session recording access
CE Credit
What You Will Learn\:
Identify Oppositional Defiant Disorder\, children at risk\, and differentiate from similar childhood diagnoses by etiology and behavior
Apply a three-step\, evidence-based approach to intervention called SimpleThree with defiant children ages 4-14
Incorporate a behavioral modification system using clear\, measurable rules to encourage good behavior and structure
Learn how to strategically follow up with families to reinforce effective parenting skills and maintain success and support with easy-to-access resources
Your Presenter\:
WARD HALVERSON\, LCSW-R\, M.Ed.\, is a licensed clinical social worker and educator with over 12 years of experience as well as a former school teacher\, army veteran and medical officer\, and father. He received a master’s degree in Social
Work from Syracuse University and a master’s degree in education from The College of Saint Rose. Mr. Halverson currently runs an outpatient mental health private practice where he specializes in the treatment of child and family
defiance\, anxiety\, and trauma\, and has developed the SimpleThree system to approach these issues with his clients as well as other mental health professionals.
Disclaimer\:
This event qualifies for one CE credit. Only registered attendees will have access to CE. A Cross Country Education web account is required to attend. There is no charge for a CCE web account. It is recommended that you join the meeting
15 to 20 minutes early. Speaker phone sound quality is poor and it is recommended that they not be used to listen to the event.
Technical requirements\:
To view this webinar you will need to download the WebEx Application. You will be prompted to download it when you first enter the site. To save time\, you can setup prior to the meeting by following this link\:
https\://apidemoeu.webex.com/apidemoeu/meetingcenter/mcsetup.php
Who Should Attend\:
Social Workers\, Psychiatric Nurses\, School Nurses\, Psychiatric Nurse Practitioners\, Licensed Professional Counselors\, Marriage and Family Therapists\, Psychologists\, Educators\, School Social Workers\, School Administrators\, Foster Care
Professionals\, Parents\, Clergy
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120225T130300Z DTEND;VALUE=DATE-TIME:20120225T130300Z UID:http://www.webinarcentral.net/content/social-enterprise-applications-webinar URL;VALUE=URI:http://www.webinarcentral.net/content/social-enterprise-applications-webinar SUMMARY:Social Enterprise Applications- Webinar DESCRIPTION:Online Event on the latest developement in Enterprise Social Cloud Applications
SugarCRM\, IBM and Zyncro will present cases how with Social apps you can benefit. Are Social enterprise apps finally delivering the productivity businesses desire by systematically grouping and rating people\, information\, and processes required to answer business needs?
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120227T150000Z DTEND;VALUE=DATE-TIME:20120227T160000Z UID:http://www.webinarcentral.net/content/global-data-transfer-solutions-%E2%80%93-complying-eu-laws-regulations URL;VALUE=URI:http://www.webinarcentral.net/content/global-data-transfer-solutions-%E2%80%93-complying-eu-laws-regulations SUMMARY:Global Data Transfer Solutions – Complying with EU Laws & Regulations DESCRIPTION:This webinar will help you understand the EU data transfer regime and the significant differences within the EU member states in relation to the way in which data transfers are permitted from the EU to other countries.
Why Should You Attend\:
The EU laws on data sharing and data transfer were drafted in an era when data moved slowly and in small quantities. The current “everywhere to everywhere” movement of data means that it is increasingly difficult for international businesses to run their affairs whilst complying with EU laws on data transfers. Corporate governance\, outsourcing\, cloud computing and social media all raise massive data protection and data transfer concerns\, and the increase in regulatory investigations and fines mean that multinationals must comply with EU data transfer laws or risk investigations and fines.
This 60-minute presentation will help you understand the EU data transfer regime and the significant differences within the EU member states in relation to the way in which data transfers are permitted from the EU to other countries.
Areas Covered in the Seminar\:
- Data transfer registration procedures.
- Exemptions from registration.
- Safe Harbor.
- EU Model Contracts for controller to controller.
- Omnibus data transfer agreements.
- Binding Corporate Rules.
- EU Model contracts for controller to processor.
This 3-hr virtual seminar on child support regulations will focus on federal and state requirements to compliantly and effectively handle child support withholding orders.
Why Should You Attend\:
Dealing with child support withholding orders can cause some of the most stressful and emotional situations that can be encountered in payroll. Not only are there severe penalties for violations of compliance rules\, making sure that they are handled correctly can help relieve the emotional pressure that can surround individual orders. The reality is that all of the people and entities involved in these situations expect action from the payroll department. And it is up to the payroll department to catch and correct any errors that have been made by anyone along the way.
This in-depth presentation focuses on the requirements to compliantly and effectively handle child support withholding orders. Federal and state requirements will be covered as well as specific issues such as what to do if there is more than one withholding order and which order has priority? What if there is not enough money to comply with the order? What do I do with the arrears?
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120227T160000Z DTEND;VALUE=DATE-TIME:20120227T173000Z UID:http://www.webinarcentral.net/content/osha-recordkeeping-recent-recordkeeping-interpretations-webinar-complianceonline URL;VALUE=URI:http://www.webinarcentral.net/content/osha-recordkeeping-recent-recordkeeping-interpretations-webinar-complianceonline SUMMARY:OSHA Recordkeeping\: Recent Recordkeeping Interpretations - Webinar By ComplianceOnline DESCRIPTION:This 90-minute OSHA Recordkeeping training class will incorporate the lessons learned from OSHA’s recent Interpretation Letters into the existing OSHA recordkeeping analysis as well as OSHA’s current Frequently Asked Questions. In this interactive program\, OSHA recordkeeping scenarios will be used so that the rules articulated in the recent Interpretation Letters can be applied to real-life factual situations that arise in your work environments.
Why Should You Attend\:
OSHA injury and illness recordkeeping compliance is a point of emphasis for OSHA\, and the recordkeeping regulations are frequently cited by the Agency.
In addition to providing instruction on how to apply the new Interpretation Letters\, this webinar training will reinforce the key concepts that must be understood for accurate OSHA recordkeeping. The presenter has audited hundreds of employers’ OSHA 300 Log recordkeeping practices\, has defended OSHA recordkeeping citations\, and is a frequent speaker and trainer on OSHA recordkeeping. The webinar is a “must” for employers preparing for the possibility of an OSHA inspection.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120227T160000Z DTEND;VALUE=DATE-TIME:20120227T170000Z UID:http://www.webinarcentral.net/content/recruiting-limited-budget-proven-low-and-no-cost-tools-and-approaches URL;VALUE=URI:http://www.webinarcentral.net/content/recruiting-limited-budget-proven-low-and-no-cost-tools-and-approaches SUMMARY:Recruiting on a Limited Budget\: Proven Low and No Cost Tools and Approaches DESCRIPTION:This Recruiting on a Limited Budget training will cover costs involved in the recruiting process and indicate areas that can be reduced or eliminated by deviating from the traditional methods used. It will focus on alternative methods to attract and find excellent hires at a lower cost.
Why Should You Attend\:
Recruiting is a costly process in both time and money. “Cost per Hire” metrics show clearly what costs are involved in the recruiting process and can also indicate areas that can be reduced or eliminated by deviating from the traditional methods used. Whether you are filling one position or expanding significantly\, there are alternative methods to attract and find excellent hires at a lower cost.
This webinar explores ways companies can recruit and hire through low and no cost methods which can result in reduced recruiting expenses and at the same time\, more successful matches to their open positions. When budgets are tight\, creativity and ingenuity pay off and there are many new ways to find the best candidates. Many of these options also are more targeted and therefore save time as well as money.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120228T150000Z DTEND;VALUE=DATE-TIME:20120228T154500Z UID:http://www.webinarcentral.net/content/iaq-ii-challenges-office-%E2%80%93-indoor-air-quality-management-1 URL;VALUE=URI:http://www.webinarcentral.net/content/iaq-ii-challenges-office-%E2%80%93-indoor-air-quality-management-1 SUMMARY:IAQ II Challenges at the Office – Indoor Air Quality Management DESCRIPTION:Indoor Air Quality Challenges at the Office
A healthy workplace starts with healthy air
A majority of workers spend 40 or more hours at the office – and poor indoor air quality can affect their performance\, productivity and well-being\, which in turn can hurt a company’s bottom line.
In this webinar\, we explore common aspects of IAQ and offer an in-depth analysis relating to air quality and the need for proper indoor air management to avoid health hazards and related complications.
Find out what you can do to improve the indoor air quality in your workplace\, what questions to ask and how a healthier work environment can benefit the employees as well as the company.
We will propose an effective\, preventive IAQ management program that addresses many areas\, including source control – ventilation – humidity control – filtration.
Join us in Part II of our Webinar Series on IAQ Management at the workplace!
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120228T160000Z DTEND;VALUE=DATE-TIME:20120228T180000Z UID:http://www.webinarcentral.net/content/dissolution-instrument-qualification-meet-requirements-and-minimize-product-oos-dissolution- URL;VALUE=URI:http://www.webinarcentral.net/content/dissolution-instrument-qualification-meet-requirements-and-minimize-product-oos-dissolution- SUMMARY:Dissolution Instrument Qualification to Meet Requirements and Minimize Product OOS Dissolution Results DESCRIPTION:This 2-hr Dissolution Instrument Qualification webinar will discuss recent FDA requirements for dissolution instrument qualification and provide practical suggestions to avoid pitfalls in performance of the tests\, minimize Performance Verification Test and product failures.
Why Should You Attend\:
This interactive course is designed to provide the participant with a knowledge of the requirements for dissolution instrument qualification\, an area which has been changing rapidly over the last few years. Both the use of USP Performance Verification Tablets and mechanical approaches will be discussed\, as well as the requirements presented in the USP and in a recent FDA Guidance. Pitfalls in the performance of the tests as well as instrument issues which are not addressed by the Qualification procedures will be addressed. Finally\, some of the practical suggestions that can minimize both PVT and product failures will be presented. There will be ample opportunity for participant questions.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120228T160000Z DTEND;VALUE=DATE-TIME:20120228T170000Z UID:http://www.webinarcentral.net/content/defending-against-ofac-investigation-webinar-complianceonline URL;VALUE=URI:http://www.webinarcentral.net/content/defending-against-ofac-investigation-webinar-complianceonline SUMMARY:Defending Against an OFAC Investigation - Webinar By ComplianceOnline DESCRIPTION:This webinar on Defending Against OFAC Investigations is designed to teach participants to successfully navigate the OFAC enforcement process and reduce any OFAC penalties.
Why Should You Attend\:
The U.S. government takes violations of economic sanctions prohibitions very seriously. Just recently\, JP Morgan Chase had to pay $88.3 million to settle allegations that it had violated a number of OFAC administered sanctions prohibitions. This type of penalty is not abnormal as for most sanctions violations OFAC can administered penalties of up to $250\,000 USD or twice the value of the transaction\, per transaction that violated the sanctions. As there is lack of information publically available many are lost when it comes down to how an OFAC investigation and enforcement action should be handled.
Defending against an investigation from the United States Department of the Treasury Office of Foreign Assets Control (OFAC) can be a stressful process. Careful navigation and understanding of this process is required to shield one’s self or company from massive penalties and reputational risk.
This webinar is designed to teach participants how to successfully navigate the OFAC enforcement process and reduce any OFAC penalties.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120228T160000Z DTEND;VALUE=DATE-TIME:20120228T173000Z UID:http://www.webinarcentral.net/content/regulatory-perspectives-clinical-project-management-meeting-fda-requirements-clinical-trials URL;VALUE=URI:http://www.webinarcentral.net/content/regulatory-perspectives-clinical-project-management-meeting-fda-requirements-clinical-trials SUMMARY:Regulatory Perspectives of Clinical Project Management\: Meeting FDA Requirements for Clinical Trials DESCRIPTION:This 90-minute webinar will provide an overview of regulatory management for clinical trials. It will discuss key regulatory aspects of a clinical project such as clinical protocol management\, IRB management\, safety reporting\, rules for recruitment programs\, seeking advice from FDA\, trial master files\, and training requirements.
Why Should You Attend\:
Clinical Project Managers need to have clear perspective of what may be needed for assuring compliance with FDA requirements of a given clinical trial at all times. Non-compliance with these requirements could lead to rejection of the trial data\, and even other more severe penalties.
This course will provide an overview of regulatory management for clinical trials. We would discuss the key regulatory aspects of a clinical project such as clinical protocol management\, IRB management\, safety reporting\, rules for recruitment programs\, seeking advice from FDA\, trial master files\, and training requirements. Practical tips for regulatory management of a clinical trial project will be provided using case studies from the presenter’s personal experience. If you are aspiring to be a clinical project manager\, are sponsoring a clinical trial\, supervise clinical trial operations\, or would like to become a clinical site\, this course is a must for you.
Learning Objectives\:
At the end of this webinar\, the attendees will be familiar with the following\:
- Most common regulatory issues for clinical trial management.
- Documents required for FDA submission and trial master files.
- Processes to seek and document management decisions with regulatory implications.
- Do's and Don'ts for regulatory management of a clinical trial.
Please join Estuate and Triple Point Technology to learn more about solutions around Oracle Integration using Oracle Fusion Middleware\, SOA and BPEL and how we can help you\:
Register and attend the webinar to be eligible for a no-charge assessment to help quantify the costs and benefits of Integration with Oracle Fusion Middleware.
Date \: Tuesday\, February 28\, 2012
Time \: 10AM PST
Obtain a Master’s degree in International Human Resources Management (HRM) while gaining valuable professional experience in a leading international company based in France.
This will be an informative Webinar of CIFFOP International Human Resources Management Master Degree.
Multinational companies need well trained and seasoned operational HRM officers. This programme will help you acquire the necessary HRM skills and develop concrete experience in an international setting.
Join this webinar with Web2Present and find out everything that you want to know about the Application Requirements &\; Selection Process.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120228T171800Z DTEND;VALUE=DATE-TIME:20120228T171800Z UID:http://www.webinarcentral.net/content/master-international-human-resources-management-paris URL;VALUE=URI:http://www.webinarcentral.net/content/master-international-human-resources-management-paris SUMMARY:Master of International Human Resources Management in Paris DESCRIPTION:Obtain a Master’s degree in International Human Resources Management (HRM) while gaining valuable professional experience in a leading international company based in France.
This will be an informative Webinar of CIFFOP International Human Resources Management Master Degree.
Multinational companies need well trained and seasoned operational HRM officers. This programme will help you acquire the necessary HRM skills and develop concrete experience in an international setting.
Join this webinar and find out everything that you want to know about the Application Requirements &\; Selection Process.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120228T133000Z DTEND;VALUE=DATE-TIME:20120228T143000Z UID:http://www.webinarcentral.net/content/free-webinar-oracle-iprocurement-oracle-purchasing-application URL;VALUE=URI:http://www.webinarcentral.net/content/free-webinar-oracle-iprocurement-oracle-purchasing-application SUMMARY:Free Webinar - Oracle iProcurement in Oracle Purchasing Application DESCRIPTION:Oracle iProcurement is a self service based requisitioning application that controls employee purchasing. It is a key component of oracle advanced procurement\, the integrated suite that dramatically cuts all the supply chain management (SCM) costs. The Oracle iProcurement functionality provides the essentials for the ordering portion of the procurement process. This includes catalog content management\, requisitioning\, purchase order creation\, and receiving orders. This webinar will deal in brief about the benefits and usages of Oracle iProcurement.
Agenda\:
- Procurement process\: Oracle iProcurement
- Indirect and Direct Sourcing
- Why are we switching to iProcurement?
- Various Benefits
- Oracle iProcurement Release 12 Enhancements
- Oracle iProcurement Overview
- Oracle iProcurement in Comprehensive Procure-to-Pay Flow
- Core Features of Oracle iProcurement
- Oracle Service Procurement Integration
Free Registration\: https\://www1.gotomeeting.com/register/285879993
Read More\: http\://www.iwarelogic.com/resources/webinars/oracle-iprocurement-in-orac...
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120229T140000Z DTEND;VALUE=DATE-TIME:20120229T150000Z UID:http://www.webinarcentral.net/content/dmr-dhr-what-really-required-webinar-complianceonline URL;VALUE=URI:http://www.webinarcentral.net/content/dmr-dhr-what-really-required-webinar-complianceonline SUMMARY:DMR & DHR - What Is Really Required - Webinar By ComplianceOnline DESCRIPTION:This 90-minute training will discuss the FDA's QSR requirements for a Device Master Record (DMR) and how you can use it to build your Device History Record (DHR). You will learn what to keep in each record and organize them to help you lower cost in the QMS and provide valuable information when you need to investigate a problem and take corrective action.
Why Should You Attend\:
Have you ever been confused about what needs to be in your Device Master Record (DMR) and your Device History Record (DHR)? This webinar will help you understand the requirements and assemble a complaint DMR and use it to build your DHR.
The webinar will also help you understand some very important related documents. The Design History File (DHF) is part of the design project\, and does not duplicate the DMR. The webinar will help you understand the difference. In addition\, the Quality System Record (QSR) can be a valuable adjunct to the DMR. The speaker will advise you on when to put device information into the QSR.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120229T160000Z DTEND;VALUE=DATE-TIME:20120229T173000Z UID:http://www.webinarcentral.net/content/solutions-challenges-phase-i-and-fim-studies-today%E2%80%99s-world URL;VALUE=URI:http://www.webinarcentral.net/content/solutions-challenges-phase-i-and-fim-studies-today%E2%80%99s-world SUMMARY:Solutions to the Challenges of Phase I and FIM Studies in Today’s World DESCRIPTION:This 90-minute webinar will help you identify the challenges in Phase I and FIM studies and present solutions on how to overcome these challenges.
Why Should You Attend\:
As need for more aggressive drug development that still ensures the safety of the subjects and the drug itself becomes more and more important\, the challenges of those individuals responsible for the Phase I activities increase exponentially. To not meet these challenges has consequences.
The lines of distinction between the classical phases in the drug development are becoming more and more blurred\, and the challenges facing the Sponsor\, the Principal Investigator\, and the sites are becoming increasingly important. No longer is the First-in-Man study only done on normal healthy volunteers or are protocols fixed lines in the sand that are not changeable until the study is completed. No longer is the New Chemical Entity (NCE) a simple chemical with almost predictable effects and we no longer see Phase I studies conducted only in confined Clinical Pharmacology Units. All of these challenges make recruiting more challenging and Monitoring equally so.
The answer is to identify the challenges and keep up with the changing environment in the development of these NCE’s in ever more complex and serious diseases so that the DRA’s find nothing to shut you down for. The focus of this 90-minute webinar is how to overcome the challenges in Phase I and FIM studies.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120229T170000Z DTEND;VALUE=DATE-TIME:20120229T170000Z UID:http://www.webinarcentral.net/content/how-create-strong-verbal-brand-job-market URL;VALUE=URI:http://www.webinarcentral.net/content/how-create-strong-verbal-brand-job-market SUMMARY:How to create a strong verbal brand in this job market? DESCRIPTION:Corp-Corp.com cordially invites you to join a Technology related webinar on title “How to create a strong verbal brand in this job market?”
Benefits of the webinar\:
Most technology professionals come up short when it comes to verbalizing their message. From their resume\, to their LinkedIn Profile\, to how they project their message when applying for jobs leaves much to be desired. This webinar is about creating what has now come to be known as an Inductive Resume to project a verbal message that stands above the crowd and gets attention. Learn how to write a resume that gets noticed\, how to create a LinkedIn Profile that attracts recruiters to it\, and how to go after a job that you thought was out of your reach!
Speaker's Profile\:
Webinar will be presented by Dilip Saraf\, LinkedIn’s #1 Career Coach. He left the corporate world as head of engineering of high-tech company nearly 25 years back and has gone through four very different careers since then. As a career coach he has worked with over 5\,000 clients globally in a variety of industries and authored five books (his sixth one is in it’s final stages) and countless blogs on career management\, job search\, leadership\, and re-invention. Dilip resides in the Silicon Valley and works with clients globally. Registration\:
To register for this webinar\, Visit http\://www.corp-corp.com/blog/create-strong-verbal-brand-jobmarket/?aid=...
There will be an opportunity to ask your questions and doubts at the end of the webinar. Register now and join with us. Feel free to forward this message to your friends and colleagues.
END:VEVENT BEGIN:VEVENT DTSTAMP;VALUE=DATE-TIME:20120524T184845Z DTSTART;VALUE=DATE-TIME:20120229T134000Z DTEND;VALUE=DATE-TIME:20120229T143000Z UID:http://www.webinarcentral.net/content/preserving-customizations-overlays-custom-objects-ar-system-7604-deep-dive-session URL;VALUE=URI:http://www.webinarcentral.net/content/preserving-customizations-overlays-custom-objects-ar-system-7604-deep-dive-session SUMMARY:Preserving Customizations with Overlays & Custom Objects in AR System 7.6.04\: Deep-dive Session DESCRIPTION:Join this webinar on Wednesday\, 29th February\, 2012
Time\: 7\:00 pm – 8\:00 pm IST
Register Here\: https\://www1.gotomeeting.com/register/419445329
This webinar will cover a deep-dive session on Preserving Customizations with Overlays and Custom Objects in AR System will describe why we need to go for Overlay\, using Best Practice Conversion Utility (BPCU)\, how we can identify and preserve customizations while future upgrades and avoid business impact in terms of time and money.
AGENDA
Introduction
Why Overlay?
Benefits of overlays
What is Best Practice Conversion Utility (BPCU)?
Using Best Practice Conversion Utility
Questions