News

FDA Probes Death Of 8-Year-Old Who Received Sarepta's Elevidys
The U.S. Food and Drug Administration (FDA) announced on Friday, after market close, that it is investigating the death of an ...
Futurism on MSN3d
The FDA Is Using an AI to "Speed Up" Drug Approvals and Insiders Say It's Making Horrible Mistakes
Insiders at the Food and Drug Administration are ringing alarm bells over the agency's use of an AI to fast-track drug ...
Is the FDA doing enough about food additives?
Food dyes are known to have a wide range of impacts on health, such as cancer risks, behavioral problems in children, and ...
ConsumerAffairs2h
Feds to industry: Help us defin ‘Ultra-Processed Food’
HHS, USDA, and FDA launch formal effort to create a national definition for ultra-processed foods. Officials say a clear ...
Food Safety News13h
FDA increases import enforcement on seafood, canned food and more
The Food and Drug Administration uses import alerts to enforce U.S. food safety regulations for food from foreign countries.
Lawmakers press FDA to target knockoff weight-loss drug
Dozens of lawmakers are urging US health regulators to crack down on the booming market for knockoff weight-loss drugs amid ...
Undark Magazine10h
The FDA Plans to Reevaluate Fluoride Supplements
The agency's new drug czar wants to reanalyze risk-benefit data on ingestible fluoride, which is recommended for many ...
Drug Store News3h
FDA approves 127 innovator and biosimilar drugs in 2024, GlobalData finds
The 2024 approvals included significant milestones in the biosimilar sector, with the FDA granting approval for the first biosimilar of Stelara, Wezlana and the first denosumab biosimilars, Wyost and ...
The FDA Just Axed 52 Food Standards – Here's What It Means for Your Groceries
The U.S. Food and Drug Administration (FDA) announced that it is "revoking, or proposing to revoke, 52 food standards after ...
The FDA is cracking down on an Indian drugmaker investigated by ProPublica last year
In a warning letter, the Food and Drug Administration said Glenmark Pharmaceuticals failed to properly investigate flaws with a generic drug that ProPublica found was linked to U.S. deaths.
Entera Bio Shares Climb as FDA Backs New Primary Endpoint in Osteoporosis Study
Chief Executive Miranda Toledano said Entera's agreement with the FDA allows Enterea to advance its clinical-development program without having to wait for FDA's qualification of the Study to Advance ...
Biotech exec George Tidmarsh picked as FDA's chief drug regulator
The U.S. Food and Drug Administration named ex-biotech exec George Tidmarsh as its chief drug regulator. FDA Commissioner ...