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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. The Webinar will held on request, the duration is approx. 30 Minutes Further Information to the Online-Seminar Learn more: www.practicepaysolutions.com/mastery Join us for a free series of one-hour webinars with the a team of industry experts! We're presenting the less-covered, critical issues for small business owners, so you can reduce the time you spend on set-up and administration-- and focus on what really matters. Can't attend live? We'll send you the call recordings so you can access valuable information and share the event with your community! April 2nd: The Joy of Productivity with George Kao April 16th: How to Create Profitable Referral Partnerships with Robert Notter April 24th: Say Bye-Bye to Your Boring Bio with Nancy Juetten May 15th: From Contacts to Contracts with Caterina Rando May 22nd: Red Fire Profitability with Liz Goodgold June 5th: Developing Contracts & Service Agreements with Tasha Cooper Coleman June 19th: Outsourcing Secrets with Travis Greenlee July 10th: Your Money Relationship = Your Business Success with Helen Kim July 24th: How to Play a Bigger Marketing Game with Fabienne Fredrickson Allan Gonsher and Kids Inc are pleased to a offer a series of Play Therapy Webinars. If your work with children, or want to work with children, these are workshops that you can not afford to miss. Each webinar workshop offers one hour of continuing education credit. Start: 06/12/2012 10:00 am
End: 06/12/2012 11:00 am
This webinar will cover essential elements of multi-national medical device clinical trials, help you understand US and non-US regulatory processes for medical device clinical trials and provide practical tips for assuring US market approval for your device. Testing of medical devices raise unique regulatory, logistical and practical issues that need to addressed for successful completion of a given trial. The biggest challenge perhaps is conducting multi-national trials with medical devices primarily because medical devices are developed and regulated very differently in the US compared to the rest of the World. This session will discuss all these issues and challenges - including the use of controls or shams, IRB review of medical device trials, patient access, informed consent issues, retrospective clinical experience data, patient access to dual-availability devices, personnel training, charging a participant for the cost of an investigational medical device, and GCP compliance -using case studies from the presenter’s extensive experience with conducting multi-national medical device clinical trials. You should attend this webinar if:
Start: 06/12/2012 10:00 am
End: 06/12/2012 11:00 am
This FDA warning letter closeout program will discuss how to successfully complete warning letter close out program which will help firm to obtain a closeout letter from FDA. Why Should You Attend: FDA Commissioner Margaret Hamburg recently announced several new enforcement initiatives. Part of the "new FDA" is the increased issuance of warning letters and the creation of a warning letter "closeout", which regulated firms can use to your advantage. FDA's warning letter program has changed substantially and more warning letters will be issued - and faster! In the past, firms that received a warning letter from FDA were subject to unending scrutiny, speculation and financial challenge. But now warning letter recipients will have the chance to prove they are back in compliance. , FDA will provide a manner for a firm to demonstrate that it has complied with the terms of an enforcement action. The warning letter closeout program has begun as of September 2009. All firms who receive a warning letter will have the opportunity to obtain a "closeout" letter from FDA. Firms that fail to obtain a closeout letter will be clearly identified as still being under FDA scrutiny. Attend this Webinar to know everything about warning letters, warning signs, issuance, company’s response and how to rectify the FDA warning letter close out mistakes. Start: 06/12/2012 10:00 am
End: 06/12/2012 10:00 am
This webinar will help you understand OSHA’s requirements for preventing accidental release of energy or accidental start-up of equipment. You will learn what documents to have in place, including a written lockout/tagout plan, and how to implement it. Why Should You Attend: Due to the significant number of fatalities, injuries, fires, spills/releases, and “near misses” in manufacturing, OSHA requires procedures for isolating energy sources and equipment startup. Due to unauthorized persons trespassing or accidentally accessing the area and multiple employers working on these projects they are a significant target for lawsuits for accidental releases of energy or startups. Plaintiff attorneys target the failure of parties responsible for isolating energy sources and controls. Unfortunately, in most cases defendants were not aware of the OSHA requirements until it is too late. In 2011 lockout/tagout ranked 5th in the most common OSHA citation with 3,756 violations. This webinar will help you understand OSHA’s requirements for preventing accidental release of energy or accidental start-up of equipment. You will learn what documents to have in place, including a written lockout/tagout plan, and how to implement it. Learning Objectives:
Start: 06/12/2012 10:00 am
Overview: Major postmarketing vigilance revisions are now in force. A revised medical device guidance document on postmarketing vigilance (MEDDEV 2.12-1 rev 5) came into force on January 1, 2008. Providing more guidance than the previous version, the new document includes new reporting terminology and concepts such as "periodic summary reporting" and "trend reporting." In addition, the terms "advisory notice," "near incident," and "recall" have been eliminated or replaced. Although MEDDEVs are not legally binding, it is likely that all European Competent Authorities will follow the new guidelines and will expect organizations involved in the management and reporting of adverse incidents to follow them as well. This session will address topics such as new definitions; the guideline's extended scope, reporting criteria/timelines, filing safety notices and field safety corrective actions, and more. The new guidelines contain some controversial aspects, including the extension of their scope and the new approach of immediate reporting unless delays can be justified. However, they also provide additional clarity and more-detailed advice in many areas. The European Database EUDAMED also is described. Periodic or trend reporting under certain conditions is now allowed, as a result of the integration of certain GHTF concepts. Although a transition period was allowed until the end of 2007, the revised guidelines will undoubtedly result in the need for manufacturers, authorized representatives, and distributors to make changes to their SOPs and other documents. Price List: webinars@globalcompliancepanel.com Phone: 800-447-9407 Start: 06/12/2012 10:00 am
End: 06/12/2012 11:30 am
This 90-minute webinar will discuss the requirements, the risks, and the issues in using mobile devices and social networking for patient communications. We will review policies and procedures, documentation, major compliance areas and training to ensure they are updated to meet these new challenges. Why Should You Attend: Most HIPAA covered entities now face difficult choices as mobile devices such as smart phones and tablets proliferate and become the standard for personal communications both by providers and their patients, and social networking sites become a preferred means of communication for many. Have you updated your information security risk analysis or policies and procedures to address the increasing use of mobile devices and social networking for patient communications? If not, you run the risk of breaches, rule violations, and fines in the event of mishandling of PHI using these new technologies. With the new HIPAA random audit program now getting under way, and increases in enforcement actions following breaches, now is the time to ensure your organization is in compliance with the regulations and meeting the communication needs and desires of its providers and patients. You need the proper privacy protections for health information, and the necessary documented policies and procedures, as well as documentation of any actions taken pursuant to your policies and procedures. Your policies and procedures will probably need major revisions to maintain compliance in areas such as individual access of records, accounting of disclosures, and breach notification. And, of course, you will need to train your staff in all the new policies and procedures. Learning Objectives:
Start: 06/12/2012 10:00 am
Overview: 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. Understanding the different techniques, their limitations, and proper execution will result in more accurate and precise moisture results, which translates into better quality products with longer shelf lives. Why you should attend: 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. Additionally, 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: Who Will Benefit: This webinar will provide valuable assistance to those companies involved in the handling of powders, lyophilized products, solid pharmaceutical dosage forms, and dried foods. Price List: webinars@globalcompliancepanel.com Phone: 800-447-9407 Start: 06/12/2012 11:00 am
Historically, studies have shown a strong correlation between increased levels of student engagement and higher overall graduation rates. In this brief 40-minute Webinar, GoingOn Networks will highlight initiatives at Penn and ASU that are creating engaging online experiences for faculty & research collaboration, first year student experience and more effective informal learning environments. In this session you will learn how to: To register, visit http://www.goingon.com/free-webinar-leveraging-social-modalities-engage-... Start: 06/12/2012 1:01 pm
The terms Fair Lending and UDAAP tend to strike fear and panic in the hearts of many financial industry professionals due to their over-arching and vastly subjective interpretations. Unlike more "traditional" regulations these two fundamental pillars of ethical banking interweave the grey areas that connect the regulatory environment with risk management. The end result is a veritable mine field for even the most seasoned financial industry professionals when it comes to balancing successful business operations and consumer protection. The goal of this webinar is to help demystify these terms and provide you with a better way forward for managing the risks associated with these aspects of consumer protection. Why should you attend: Current and future compliance professionals, lenders, loan originators, board of directors, senior management. Anyone responsible for the development, marketing, and sales of bank products or services. Webinar Includes: Q/A Session with the Expert to ask your question PDF print only copy of PowerPoint slides 90 Minutes Live Presentation Areas Covered in the Session: The goal of consumer protection rules in banking The risk scenarios UDAAP and Fair Lending create The hidden simplicity of UDAAP and Fair Lending risk management The pratfalls of consumer protection The synergy between Fair Lending, UDAAP and your business goals. Who will benefit: (Titles) Board of Directors Members About Speaker Asaad A. Faquir is currently a Compliance Officer for a growing community bank in New England. He began his career in banking as an Operations and Management Consultant for a large multi-billion dollar bank in South Florida. Asaad has a BS in Finance from Florida State University, an MBA in Finance from Temple University and a Masters Degree in Human Resource Management from the University of Limerick in Limerick, Ireland where he focused his Masters Thesis on Strategic Leadership, while attending school as a Rotary International Ambassadorial Scholar. Asaad has conducted successful webinars in the areas of risk and compliance and has been an Adjunct Professor of Human Resource Management. Start: 06/12/2012 2:00 pm
This one-hour webinar provides attendees with a definition of art therapy, its benefits, & how it differs from verbal therapy. Case studies will be presented to assist attendees in identifying indicators & key images in their clients’ art. Full Description: treatment is addressed through assessment by examining age-appropriate drawing skills and the symbolism of images that have personal meaning to our clients. In addition, this course examines art-making as personal growth and its therapeutic benefits. The attendees will learn specific indicators to look for in their clients’ art work and how to identify key images through the presentation of several case studies. Through these case studies the participants will identify how clients can express their mood through drawing and painting. Psychological and behavioral problems, such as regression and impairments, will be identified through the symbolism in clients’ art work. Course Includes: What You Will Learn: Your Presenter: 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. For the past 15 years, Ms. Hayes has worked in numerous psychiatric settings. 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: 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: time, you can setup prior to the meeting by following this link: https://apidemoeu.webex.com/apidemoeu/meetingcenter/mcsetup.php Who Should Attend: Pediatricians, Physicians, Art Therapists, Pastoral Counselors, Guidance Counselors, Youth Pastors, Youth Counselors, Educators Start: 06/12/2012 3:00 pm
Amidst all the debates about the value of social media influence and reputation measures such as a Klout, little attention has been given to where such metrics are undoubtedly valuable - on organizations´ own social networks. Two critical elements of successful enterprise social networking adoption are measurement and incentivizing participation. Influence and reputation scores on enterprise social networks help users: Clearvale provides visibility and metrics to develop and nurture an active enterprise social network. This unique set of metrics is designed to measure network usage and assess the value of contribution from all participants. This webinar introduces you to the topic of using social analytics to measure reputation and influence. Join the discussion (or listen in) and we look forward to seeing you online! Start: 06/12/2012 10:46 pm
regulatory requirements are met. This concept is codified in both the QSR and ISO 13485. FDA officials have repeatedly stated that the management controls subsystem is the central subsystem because it is the "glue that holds the quality system together." Since it is individuals in top management that the FDA will typically seek to fine or prosecute in the event of major noncompliance, this session is key for those individuals who are members of top management, or those regulatory professionals who need to understand these requirements to assure top management is fulfilling its responsibilities. This session will discuss the requirements for Management Controls, including organizational structure, internal audits, establishment of a quality policy and confirmation it is being followed, establishment and contents of a quality system and quality plan, and of course all aspects of management reviews. Areas Covered In the Seminar: Who will benefit: Price List: webinars@globalcompliancepanel.com Phone: 800-447-9407 | ||
