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Eli Lilly Alzheimer’s drug gets FDA panel date after approval delay
The Hill via AOL· 4 hours agoAn outside panel of advisers to the Food and Drug Administration (FDA) will meet next month to...
FDA panel to consider MDMA for PTSD treatment
NBC NEWS· 4 hours agoThe Food and Drug Administration's panel of independent advisers will on June 4 deliberate whether they should recommend approval for the first...
FDA sets date for advisory meeting on Lilly’s closely watched Alzheimer’s drug
BioPharma Dive via Yahoo Finance· 8 hours agoDive Brief: The Food and Drug Administration has finalized the date when an outside group of experts...
Weight loss drug shortage: Zepbound and Wegovy in short supply, says FDA
BenefitsPRO· 5 days agoThe U.S. Food and Drug Administration updated its drug shortage database in April to reflect that...
US FDA panel to discuss Eli Lilly Alzheimer's drug on June 10
Reuters via Yahoo News· 5 hours agoFood and Drug Administration's approval last year. Lilly's donanemab was declined accelerated...
Reform of Federal Marijuana Law and Potential Impacts on State Medical Marijuana Programs | The...
Law.com· 3 hours agoRegardless of how marijuana is rescheduled under federal law, the Food and Drug Administration (FDA)...
FDA Experts Weigh In On Incannex's CannQuit-O With Feedback On CBD As Treatment For Opioid Use...
Benzinga· 3 hours agoIncannex Healthcare Inc. IXHL, a cannabinoid and psychedelic medicine biotechnology company,...
2 Planters nuts products recalled over possible listeria
Deseret News via Yahoo News· 2 hours agoFood and Drug Administration. The recall includes 4-ounce packages of Planters Honey Roasted...
FDA approves Geneoscopy’s ColoSense test for CRC screening
Medical Device Network via Yahoo Finance· 9 hours agoThe US Food and Drug Administration (FDA) has granted approval to Geneoscopy's ColoSense, a...
FDA’s Final LDT Rule Is Here, and the Changes Show the Agency Is Serious and Actually Listening to...
The National Law Review· 1 day agoThe Food and Drug Administration (FDA) published its final rule on laboratory developed tests (LDTs)...