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: 07/03/2012 7:10 am
Overview: Medical device firms need to be aware of the benefits of compliance as well as the dangers of inadequate complaint handling. This Webinar will explain the regulatory process and in understandable terms.
Many medical device firms face regulatory issues as a result of inadequate complaint handling. FDA has explicit complaint handling requirements and poor complaint & reporting procedures often result in costly recalls and warning letters. FDA warning letters and recalls are posted on FDA's website and published in trade magazines, newspapers available to firm's competitors, and has even driven the firm's stocks down. This presentation will review the regulations and point out some of the pitfalls in complaint handling and reporting.
Areas Covered in the Session:
Last Chance to register on Best Practices for Medical Device Reporting (MDR), Recall, Reports of Corrections and Removals By Compliance2go
Start: 07/03/2012 1:00 pm
End: 07/03/2012 2:00 pm
Why should you attend :
If you don’t know the answers to the following questions, you should attend the seminar:
· What are the applicable federal statutes and regulations governing medical device reporting, recalls and reports of correction and removals?
Q/A Session with the Expert to ask your question
This webinar is intended to help you get familiar with the Medical Device Reporting (MDR), Recall, Reports of Correction and Removals.
In the United States, since December 13, 1984, the Food and Drug Administration (FDA) Medical Device Reporting (MDR) regulations have required firms who have received complaints of device malfunctions, serious injuries or deaths associated with medical devices to notify FDA of the incident. MDR is the mechanism for the FDA to receive significant medical device adverse events from manufacturers, importers and user facilities, so they can be detected and corrected quickly. Device firms are also subject to compliance to the FDA regulations of device recalls, correction and removals. To achieve compliance and to remain compliant, it is critical to understand how to define, document and implement the procedures for MDR, recalls, corrections and removals.
This webinar is aimed at helping device industry understand how to establish procedures for MDR, recalls, corrections and removals and further provide practical and actionable perspectives by increasing awareness and familiarity of the regulatory requirements.
Areas Covered in the Session:
Review of Relevant Statutes and FDA regulations
Who will benefit: (Titles)
Dr. David Lim obtained his Ph.D. in biological sciences at the University of Missouri-Columbia and published his thesis research in the prestigious journal “Science.” Since then, he has held various positions at Duke, US National Laboratories, Intrexon Corporation, Terumo, US FDA/CDRH, and EraGen Biosciences (A Luminex Company). In 2009, Dr. Lim served as a panel member during the FDA’s Transparency Public Meeting. Prior to founding his own consulting firm, Regulatory Doctor, Dr. Lim was Senior Vice President of Scientific and Regulatory Affairs at Aquavit Pharmaceuticals. Regulatory Doctor provides practical, actionable and strategic solutions integrated with emotional intelligence (EQ) skills for all aspects of global regulatory, quality, clinical and compliance matters. Dr. Lim has analyzed over 1,000 FDA warning letters, attended more than 50 FDA Advisory Panel Meetings, and analyzed the subject matters and decision-making processes in detail. He is familiar with more than 200 medical devices, IVD products, biologics, drugs and combination products. Dr. Lim is a certified professional for regulatory affairs (RAC) and also is a certified quality auditor (CQA) by the American Society for Quality (ASQ). He is an auditor, regulatory coach, consultant and instructor for global matters pertaining to regulatory affairs, regulatory compliance, quality and clinical affairs.