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FDA modifies strain recommendation for fall COVID vaccine amid variant shifts, uptick in cases
Center for Infectious Disease Research and Policy· 20 hours agoOn June 5, the FDA's vaccine advisory group recommended a switch to the JN.1 variant, though it held...
FDA joins international push for transparency in AI development
FierceBiotech· 22 hours agoThe FDA is joining hands with regulators in Canada and the U.K. on policies to ensure transparency...
FDA, DOJ form task force to fight illegal vapes
Medical Xpress· 4 days agoIn launching the newly created task force, the FDA aims "to coordinate and streamline efforts to bring all available criminal and civil tools to bear...
Pharma Stock Roundup: FDA Panel Endorses LLY's Donanemab, PFE's DMD Therapy Study Fails
Zacks· 1 day agoAn FDA panel endorses Eli Lilly's (LLY) Alzheimer's disease drug, donanemab. Pfizer's (PFE) DMD study on investigational gene therapy fails.
FDA warns consumers about paralytic shellfish poisoning in some contaminated shellfish
Consumer Affairs· 1 day agoThe U.S. Food and Drug Administration (FDA) has issued a warning to restaurants and retailers to put...
Co-Diagnostics seeks FDA clearance for COVID-19 test By Investing.com
Investing.com· 21 hours ago(NASDAQ:CODX), a molecular diagnostics company, has announced the completion of their first...
FDA tags Megadyne paediatric return electrode recall as Class I
Medical Device Network via Yahoo Finance· 23 hours agoClass I indicates the agency's most serious designation for a recall, meaning continued use of the...
FDA took months to react to complaint about Abbott infant formula factory, audit finds
WSB Radio· 2 days agoThe Department of Labor received the email and three days later forwarded it to an FDA address...
FDA advises Covid vaccine makers to target KP.2 for fall shots
NBC NEWS· 2 days agoThe announcement came just over a week after an FDA advisory panel voted unanimously to recommend...
FDA Took Months to React to Complaint About Abbott Infant Formula Factory, Audit Finds
US News & World Report· 2 days agoThe Department of Labor received the email and three days later forwarded it to an FDA address specifically for such complaints. The episode is one of several that led the ...