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Bristol Myers' (BMY) Krazati Gets FDA Nod for Colorectal Cancer
Zacks· 20 hours agoFree Report) announced that the FDA has approved a label expansion of its oncology drug Krazati (adagrasib). The FDA granted accelerated approval to Krazati ...
FDA's Move to OK First Menthol Vapes Is Big Mistake, Health Advocates Say
US News & World Report· 14 hours ago"The FDA’s decision today to authorize the sale of four menthol-flavored e-cigarettes made by Njoy -- the first time the agency has...
FDA warns company selling products with human fecal matter without approval
KSL Salt Lake City· 20 hours agoThe United States Food and Drug Administration has issued a warning letter to a company that appears...
FDA Issues Final Rule on Regulation of Laboratory Developed Tests | JD Supra
JD Supra· 18 hours agoAfter many years of anticipation and various congressional and agency proposals, on May 6, the Food and Drug Administration (FDA) published its final...
NC coffee shops facing nationwide recall over deadly botulism toxin risk, FDA says
Charlotte Observer· 5 hours ago“The problem was identified when the U.S. Food and Drug Administration (FDA) notified Snapchill that...
FDA OKs first menthol e-cigarettes, citing potential to help adult smokers
Associated Press via Yahoo News· 3 days agoThe Food and Drug Administration on Friday authorized the first menthol-flavored electronic...
Recalled Noodles Updated To Highest Risk Level by FDA
MSN News· 18 hours agoRecalled Noodles Updated To Highest Risk Level by FDA
FDA says Dollar Tree left lead-tainted applesauce pouches on store shelves for weeks after recall
FOX 12 Oregon· 6 days agoThe FDA sent a warning letter to Dollar Tree this month and placed Negasmart, the Ecuadorian...
FDA OKs first menthol e-cigarettes, citing potential to help adult smokers
CNBC· 3 days agoThe Food and Drug Administration on Friday authorized the first menthol-flavored electronic...
FDA’s Sarepta decision could represent ‘new way of thinking’ for agency - Boston Business Journal
The Business Journals· 1 day agoLast week the FDA expanded its previous approval for Sarepta Therapeutics’ gene therapy to treat Duchenne muscular dystrophy. Elevidys won accelerated approval from the federal ...