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Social Media Guidance Gives Drug Firms A Pass On User Content

 
• By Brenda Sandburg

The draft guidance outlines substantial reporting requirements for websites that firms control and for content on third-party sites – as well as saying when FDA intends to use enforcement discretion.

FDA’s draft guidance identifying interactive promotional materials that require agency review states that firms generally will not be responsible for the statements consumers make on their social media sites.

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More from North America

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• By Sue Sutter

Tracy Beth Høeg, who is reportedly re-examining Novavax’s COVID vaccine application, is the FDA rep at the CDC panel’s first meeting under the Trump Administration. She raised concerns about routine use of Jynneos for adolescents at risk of mpox and questioned how Moderna assessed efficacy of its COVID vaccines.