U.S. FDA

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Silver Spring, MD

U.S. FDA
@FDA
Sep 4
High standards must apply to every trial, wherever it might be conducted. The FDA is expanding oversight of foreign clinical trial sites, adding inspection resources, and increasing scrutiny of data from sites we cannot access. biospace.com/fda/fda-raises…
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U.S. FDA
@FDA
Sep 2
Clinical trial data — wherever collected — must be reliable, inspectable, and ethically derived. If FDA can't inspect a site, that's a material factor in your regulatory strategy, not a footnote. Good clinical practice protects patients. The FDA will enforce it.
Made with AI
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U.S. FDA
@FDA
Aug 31
We’ve teamed up with the @SECGov via a new Memorandum of Understanding to enhance cooperation across the life sciences sector. Greater transparency strengthens accountability and boosts regulatory predictability—meaning patients win. Read more:
SEC and FDA Announce MOU to Bolster Cooperation and Ensure Market Integrity
From sec.gov
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U.S. FDA
@FDA
Aug 27
Great news from @GeneralMills – they've completed the removal of certified color from their entire U.S. cereal portfolio and are on track to remove them from all U.S. retail products by 2027! Who’s next?
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U.S. FDA
@FDA
Aug 26
📢 FDA is hosting a public hearing on the potential future therapeutic use of psychedelic drugs in supervised and supportive settings. Topics include provider training, patient safety, access, and data standardization. Register & learn more: fda.gov/news-events/fd…
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