FDA Unveils Draft Social Media Guidance for Drug, Device Makers

The FDA released long-awaited draft guidance on the use of social media by drugmakers and medical device manufacturers. The draft guidance would require such firms to disclose the benefits and potential risks of their products when posting on social media and details how they should address and correct misinformation posted by third parties. New York Times et al.More

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Challenges...
http://jamia.bmj.com/site/icons/amiajnl8946.pdf
  • patient safety should trump all other values; corporate concerns about liability and intellectual property ownership may be valid but should not over-ride all other considerations;
  • transparency and a commitment to patient safety should govern vendor contracts;
  • institutions are duty-bound to provide ethics education to purchasers and users, and should commit publicly to standards of corporate conduct; and
  • vendors, system purchasers, and users should encourage and assist in each others’ efforts to adopt best practices.

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Benefit from new technologies... enable people to have remote access to CBT

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