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Off-Label Promotion of Medical Devices: Maximizing Your Performance Claims within FDA's Framework of Acceptable Practices - Webinar By GCPanel

 
  February 17, 2011  
     
 


GlobalCompliancePanel, Online Training Webinar
2011-04-13


Overview: The webinar covers "Off-label statute" and the FDA's nonbinding off-label guidance as relates to re-prints, performance claims, and Promotion.

Emphasis is placed on ethical, moral, and legal expectations from the FDA. You will improve your understanding of regulatory expectations for your products and improve promotional compliance for released products. The webinar is designed to help attendees understand the "off-label statute" and its legal implications. It is is also designed to help attendees operate within off-label promotional guidance, or framework.

It is illegal to market a device for the purpose that it has not been approved for by the FDA. This webinar provides guidelines set by the FDA for off-label promotion.

Areas Covered In the Seminar:
  • Off-label statute
  • Label claims
  • Allowable reprints
  • Promotional compliance
  • FDCA: The law
Who will benefit:
  • Sales executives in Medical Device
  • Regulatory Affairs personnel
  • Executives
  • Corporate counsel
  • Quality personnel
  • Directors
 
 
Organized by: GlobalCompliancePanel
Invited Speakers: Mr. Muchemu has over fifteen years experience in Medical Device, Pharmaceutical, Biomedical and Tissue industries as CAPA Training Instructor, Process validation Instructor, Change control Instructor, and CGMP consultant. He has held major positions at Abbott labs, Genentech, Boston Scientific, and Johnson and Johnson. He holds degrees in Biology, Chemical Engineering, and is currently working an MBA with a concentration in Public Health. He is an established author of several GMP books.
 
Deadline for Abstracts: 2011-04-13
 
Registration: Price List:
Live : $245.00
Corporate live : $995.00
Recorded : $295.00
E-mail: webinars@GlobalCompliancePanel.com
 
   
 
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