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FDA Draft Guidance on Risk Information in Prescription Drug & Medical Device Ads, Promotional Labeling

  • By: www.fda.gov
  • Date: November 18, 2011
Webinar All Access Pass Subscription Abstract:

The FDA has issued a draft guidance document on how manufacturers should present risk information in promotional material and ads for prescription drugs and medical devices. It describes the factors that the agency takes into consideration when evaluating ads and promotional labeling for prescription drugs and medical devices.

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