3-Hour Virtual Seminar on FDA's Scrutiny of Social Media Promotion

In this webinar you will Learn how to navigate through FDA requirements, Ways to manage your presence in social media, How to identify an off-label problem and corrective action.

Casper Uldriks
Instructor:
Casper Uldriks
Duration:
3 Hours
Product Id:
502653
Access:
6 months

More Trainings by this Expert

Price Details
$340 Recorded
$540 Corporate Recorded
Price Detail Options
Overview:

FDA steadily expands the scope and restrictions for promotion of products under its jurisdiction. Whatever and where ever to want to talk about your product, just assume your talking to FDA.

Trolling for off-label information in social media, scrutiny of educational material under "safe harbor" and apparent conflicts of interest at a public event create a sink hole for firms even though it may seem innocent in your eyes.

Facebook, Twitter or chat rooms can be rampant with off-label information. You even may be surprised about what people are saying about your product. Does FDA hold you accountable?

Why should you Attend:

  • Limitations on commercial free speech
  • Avenues of off-label information
  • Working in a "safe harbor" for off-label information distribution
  • Social media and your regulatory responsibilities
  • Correcting off-label information
  • Factoring in cognitive psychology

Areas Covered in the Session:
  • Learn to navigate through FDA requirements
  • Understand that your right to free speech is limited
  • How to get around FDA prohibitions
  • Ways to manage your presence in social media
  • How to identify an off-label problem and corrective action
  • Under how FDA applies cognitive psychology principles

Who Will Benefit:
  • Regulatory Directors
  • Marketing Directors
  • Quality Systems Auditors
  • Recall Managers
  • In-house Legal Counsel
  • Customer Support Staff
  • Sales Staff


Speaker Profile
Casper (Cap) Uldriks, through his firm "Encore Insight LLC," brings over 32 years of experience from the FDA. He specialized in the FDA's medical device program as a field investigator, served as a senior manager in the Office of Compliance and an Associate Center Director for the Center for Devices and Radiological Health. He developed enforcement actions and participated in the implementation of new statutory requirements. His comments are candid, straightforward and of practical value. He understands how FDA thinks, how it operates and where it is headed. Based on his exceptionally broad experience and knowledge, he can synthesize FDA's domestic and international operational programs, institutional policy and thicket of legal variables into a coherent picture. Professional credentials: JD - Suffolk University, licensed in Massachusetts and the District of Columbia; M.Div in psychology - Boston University with internship through Harvard University.




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