For more than a decade, the Food and Drug Administration (FDA) has made diversity in clinical trials a focus, including by issuing guidance, ...
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Hosted on MSNFDA grants orphan drug status to Arbor Biotechnologies’ PH1The US Food and Drug Administration (FDA) has granted orphan drug designation (ODD) and rare paediatric disease designation (RPDD) to Arbor Biotechnologies' gene editing therapeutic, ABO-101, to treat ...
The U.S. Food and Drug Administration (FDA) issued a final guidance for industry titled Action Levels for Lead in Processed Food Intended for ...
The recall announced in January involves contaminated broccoli sold in 20 states. Here's everything you need to know ...
The number of hospitalizations and deaths from foodborne illness doubled last year compared to 2023 in the U.S.
The U.S. Food and Drug Administration has labeled the broccoli recall as a Class I, the highest risk level issued by the ...
The U.S. Food and Drug Administration approved a new non-opioid pain medication developed by the Massachusetts-based company ...
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HealthDay on MSNFDA Approves Symbravo for Acute Treatment of Migraine in AdultsThe U.S. Food and Drug Administration has approved Symbravo (meloxicam and rizatriptan) for the acute treatment of migraine ...
(Scott Olson/Getty Images) In the final days of the Biden administration, the Food and Drug Administration proposed ... including the FDA and the Centers for Disease Control and Prevention ...
The FDA will allow two biotechnology companies to run clinical trials: United Therapeutics and eGenesis. United Therapeutics ...
Multiple people have fallen ill after consuming mini pastries contaminated with Salmonella, according to the U.S. Food and ...
Blue Ridge Beef is recalling 5,700 pounds of its 2-pound log Natural Mix, according to the FDA, which warned that salmonella can affect animals, and there is risk to humans from handling the food, ...
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