Navigating FDA's Recent Regulation on the Use of Social Media

Duration: 90 Minutes
This webinar will help you understand in detail the application of FDA's guidance on the use of social media in presenting and promoting information about drug products and medical devices subject to FDA regulation. This is critical in order to develop the appropriate strategy, policies and procedures to ensure compliance.
FDA Guidelines
Instructor: Carolyn Troiano
Product ID: 501299
Objectives of the Presentation
  • Gain an understanding of FDA's guidance on the use of social media
  • Understand FDA's current thinking, as expressed in three draft guidance documents
  • Learn how to provide product benefit and risk information to stakeholders via social media
  • Learn how to deal with character space limitations that constrain the use of social media
  • Learn how to respond to misinformation about your company's product(s) posted by independent third-parties
  • Understand pending regulatory changes under review by the US Congress
  • Understand some of the key "pitfalls" to avoid when employing social media capability in an FDA-regulated environment
Why Should you Attend
As social media use explodes, companies in FDA-regulated industries will need to understand the current and pending regulations in order to meet compliance requirements. The attendee will be provided with the FDA's current thinking and the rationale behind it. The attendee will also learn ways to meet compliance objectives in a cost-beneficial manner.

Areas Covered
  • Pros and cons of using social media venues
  • Compliant use of Social Media in an FDA-regulated Environment
  • FDA draft guidance documents
  • Balancing benefit and risk information on social media
  • Managing character space limitations on social media
  • Managing misinformation posted by independent third-parties
  • Pending regulatory action by the US Congress
Who can Benefit
  • Information Technology Analysts
  • Marketing Managers
  • Marketing Analysts
  • Clinical Data Managers
  • Clinical Data Scientists
  • Compliance Managers
  • GMP Training Specialists
  • Consultants working in the life sciences industry who are involved in the use of social media for marketing and patient information
Topic Background
FDA has been working on crafting regulations for using social media to communicate therapeutic and safety information about pharmaceutical, biologic, medical device, tobacco and other FDA-regulated products. They are attempting to strike a balance between allowing the companies to reach out to consumers without making false claims, providing misleading information, or otherwise not providing the consumer with a fair and balanced view of a product's therapeutic value and side effects.
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Recorded Session for one participant
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How it works
Live Session - How it works
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  • The webinar joining link, username and password for joining the webinar will be updated on your OCP Account 24 hours prior to the webinar
  • Presentation handouts in Downloadable PDF format will be updated on your OCP Account 24 hours prior to the live session
  • Login to the audio conference on the scheduled date and time
  • Get answers to your queries through interactive Q&A sessions via chat at the end of the session
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account 24 hours after the completion of the session
  • Please let us know your thoughts and views at the end of the webinar, your valuable feedback will help us improve
Recorded Session - How it works
  • Login to onlinecompliancepanel with your registered username and password https://www.onlinecompliancepanel.com/login
  • Upon purchase of the recorded session a link will be updated on your OCP Account within 24 hours
  • Please click on the link to access the Recorded Session
  • Presentation handouts in downloadable PDF format will be updated on your OCP Account within 24 hours of the purchase of the product
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account after 48 hours of the product Purchase
  • Please share your valuable Feedback at the end of the session
Instructor Profile:
Carolyn Troiano has more than 35 years of experience in the pharmaceutical, medical device, tobacco and other FDA-regulated industries. She has worked directly, or on a consulting basis, for many of the larger pharmaceutical and tobacco companies in the US and Europe, developing and executing compliance strategies and programs.
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