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FDA joins international push for transparency in AI development
FierceBiotech· 16 hours agoThe FDA is joining hands with regulators in Canada and the U.K. on policies to ensure transparency...
FDA panel votes unanimously for Eli Lilly's Alzheimer's treatment
Yahoo Finance· 5 days agoThe monoclonal antibody drug, delivered through an IV monthly for up to 18 months, would be the...
FDA Panel Backs Eli Lilly's Biogen-Rivaling Alzheimer's Drug
Investor's Business Daily· 4 days agoAll 11 members of the FDA's Peripheral and Central Nervous System Drugs Advisory Committee voted...
FDA panel rejects MDMA-assisted therapies for PTSD despite high hopes from veterans
Fox News· 2 days agoA U.S. Food and Drug Administration (FDA) panel rejected MDMA-based treatments for post-traumatic...
FDA took months to react to complaint about Abbott infant formula factory, audit finds
WSLS Newschannel 10 Roanoke· 2 days agoThe Department of Labor received the email and three days later forwarded it to an FDA address...
FDA panel rejects MDMA-assisted therapies for PTSD despite high hopes from veterans
Fox News via Yahoo News· 2 days agoAn FDA panel rejected MDMA-based treatments for PTSD often used with veterans. One advocate shared...
FDA must fix “inadequate” inspection and recall policies, report says
Just Food via Yahoo Finance· 2 days agoThe complaint was sent electronically to the FDA but "not escalated to senior leadership due to a...
FDA took months to react to complaint about Abbott infant formula factory, audit finds
The News-Times· 1 day agoThe Department of Labor received the email and three days later forwarded it to an FDA address...
FDA approves AstraZeneca’s Farxiga for paediatric T2D patients
Pharmaceutical Technology via Yahoo Finance· 2 days agoThe FDA's decision was based on the randomised, double-blind, placebo-controlled T2NOW Phase III...
FDA Warning Shellfish Northwest
Anacortes American· 6 hours agoA heron stands near rocks covered with algae in Netarts Bay on Friday, June 14, 2024, in Tillamook, Ore. The U.S. Food and Drug Administration says...