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

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  • TypeWebinar
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  • Location Fremont, California, United States
  • Price
  • Date 03-03-2020
3-Hour Virtual Seminar on FDA's Scrutiny of Social Media Promotion, Fremont, California, United States
Webinar Title
3-Hour Virtual Seminar on FDA's Scrutiny of Social Media Promotion
Event Type
Webinar
Webinar Date
03-03-2020
Last Date for Applying
02-02-2020
Location
Fremont, California, United States
Organization Name / Organize By
Compliance4all
Organizing/Related Departments
Online Training
Organization Type
Organization/Company
WebinarCategory
Both (Technical & Non Technical)
WebinarLevel
All (State/Province/Region, National & International)
Related Industries

Education/Teaching/Training/Development

Engineering

Business Development

Medical/Healthcare/Hospital

Location
Fremont, California, United States

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 you should 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.

 

Event link:

https://www.compliance4all.com/webinar/-502842LIVE?channel=eventsget_2020_SEO

Contact Info

Netzealous LLC, DBA -Compliance4all

Email: [email protected]

Phone: +1-800-447-9407

Website: https://www.compliance4all.com/

Others Details

Contact Info Netzealous LLC, DBA -Compliance4all Email: [email protected] Phone: +1-800-447-9407 Website: https://www.compliance4all.com/

Registration Fees
Available
Registration Fees Details
$150
Registration Ways
Website
Address/Venue
  Online  Pin/Zip Code : 94539
Landmark
California
Official Email ID
Contact
Netzealous LLC,DBA -Compliance4all

Online

[email protected]

   8004479407    Fax No: 94539