House lawmaker raises new concerns over FDA's ultra-fast drug review program

A Democratic lawmaker is raising new concerns about a Food and Drug Administration program designed to drastically shorten ...
Endocrinology Advisor

FDA Alert: Endocrinology Drug News Roundup 2026

FDA drug alerts in endocrinology, including drug approvals, drug warnings, FDA medical device recalls, and FDA drug label ...

US FDA launches program to boost domestic drug manufacturing

By Ahmed Aboulenein WASHINGTON, Feb 1 (Reuters) - The U.S. Food and Drug Administration on Sunday began accepting requests to ...
Marijuana Moment

West Virginia And Mississippi Lawmakers Approve Psychedelics Bills To Fund Ibogaine Trials Toward FDA Approval

The West Virginia House of Delegates and Mississippi House of Representatives have both approved bills to support research in ...
ABC13 Houston

FDA recall: Erectile dysfunction drug found in honey energy supplement

The FDA issued a recall Wednesday for a honey energy supplement after an undeclared erectile dysfunction medication was found ...

Auchincloss raises new concerns over FDA’s ultra-fast drug review program

Representative Jake Auchincloss of Massachusetts took issue with the agency’s handling of the program and questioned its legal underpinnings, noting that Congress did not sign off on the plan.

Duchenne Progress Shows How the FDA Should Judge Orphan Drugs

A milestone in the treatment of Duchenne muscular dystrophy (DMD) passed recently with remarkably little public notice. That ...

FDA Moves To Bring Pharma Manufacturing Back To US With New Pilot

The FDA launched PreCheck pilot program to strengthen U.S. drug supply chain by improving regulatory predictability.

FDA opens fast-track program to speed U.S. drug plant construction

FDA PreCheck pilot aims to speed U.S. pharma plant construction and approvals for critical medicines with earlier feedback.
CURE

FDA to Review New Drug Combo for Previously Treated Metastatic Colorectal Cancer

“Exelixis Announces U.S. FDA Accepted the New Drug Application for Zanzalintinib in Combination with an Immune Checkpoint ...
Lupus Foundation of America

Update: Self-administered Saphnelo remains under FDA review in the U.S.

The U.S. Food and Drug Administration (FDA) issued a complete response letter requesting additional information from ...