Events
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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 | 6
all day
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 Start: 02/06/2012 8:00 am
End: 02/06/2012 3:00 pm
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. Start: 02/06/2012 10:00 am
End: 02/06/2012 11:00 am
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. Start: 02/06/2012
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. | 7
all day
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 all day
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. Start: 02/07/2012 10:00 am
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. Areas Covered In the Session: Price List: webinars@globalcompliancepanel.com Phone: 800-447-9407 1000 N West Street | Suite 1200 | Wilmington | DE | Zip 19801 | USA Start: 02/07/2012 10:00 am
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: 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: What You Will Learn: Your Presenter: 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: 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: https://apidemoeu.webex.com/apidemoeu/meetingcenter/mcsetup.php Who Should Attend: Abuse Counselors/Addiction Professionals, Clergy, School Administrators, Physicians, Psychiatrists, Mental Health Administrators, Special Education Teachers, College Counselors Start: 02/07/2012 10:00 am
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 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 These learning points will be explored and discussed during the webinar with examples that will support the discussion. Who will benefit: CHRO Start: 02/07/2012 10:00 am
End: 02/07/2012 11:30 am
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. Start: 02/07/2012 12:00 pm
A fresh, innovative approach to Childhood Developmental Disorders Full Description: Course Includes: What You Will Learn: Your Presenter: Disclaimer: Technical requirements: Who Should Attend: Start: 02/07/2012 1:00 pm
End: 02/07/2012 1:30 pm
4 Common Questions include: 1. What tagging does Attribution require? 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. Start: 02/07/2012 2:00 pm
End: 02/07/2012 2:45 pm
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 Start: 02/07/2012 2:00 pm
End: 02/07/2012 3:00 pm
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. One media success often leads to another. Learn how to get the publicity ball rolling for you at this webinar. | 8
all day
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 all day
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. Start: 02/08/2012 8:00 am
End: 02/08/2012 11:00 am
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: Start: 02/08/2012 10:00 am
End: 02/08/2012 11:00 am
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. Start: 02/08/2012 10:00 am
End: 02/08/2012 11:30 am
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. | 9
all day
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 all day
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. Start: 02/09/2012 9:00 am
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. Start: 02/09/2012 10:00 am
End: 02/09/2012 2:00 pm
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. Start: 02/09/2012 10:00 am
End: 02/09/2012 2:00 pm
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. Start: 02/09/2012 10:00 am
End: 02/09/2012 11:00 am
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. Start: 02/09/2012 10:00 am
End: 02/09/2012 11:00 am
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? Start: 02/09/2012 11:00 am
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: 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: What You Will Learn: Your Presenter: 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: 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: https://apidemoeu.webex.com/apidemoeu/meetingcenter/mcsetup.php Who Should Attend: Start: 02/09/2012 11:00 am
“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 For more information, please visit www.goingon.com/emory-webinar Start: 02/09/2012 2:00 pm
End: 02/09/2012 3:00 pm
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! | 10
all day
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 Start: 02/06/2012
End: 02/10/2012
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. Start: 02/10/2012 10:00 am
End: 02/10/2012 11:30 am
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. Start: 02/10/2012 10:00 am
End: 02/10/2012 1:00 pm
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. Start: 02/10/2012 10:00 am
End: 02/10/2012 11:00 am
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: 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: Start: 02/10/2012 10:00 am
End: 02/10/2012 12:00 pm
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. | 11
all day
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 |

