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In discussions with multiple potential animal health company partners to collaborate to bring Canalevia®, conditionally ...
The U.S. Food and Drug Administration released more than 200 of its so-called complete response letters from its archive on ...
The U.S. Food and Drug Administration on Thursday published more than 200 of its so-called complete response letters to ...
Used for diagnosing gastroesophageal reflux, the devices may not attach or detach correctly, potentially causing serious ...
Vita Warehouse Corp. recalled more than 40,000 bottles of Vitamin B12 supplements for possible undeclared presence of peanut.
Pro-life medical groups are urging Health and Human Services Secretary Robert Kennedy Jr. to reexamine the FDA’s broad ...
Beyond staff cuts, the departures of some longtime investigators in recent months have left less experienced people tasked ...
HHS sent an email to staff members that included a "whistle-blower questionnaire," and asked them to report cases of ...
The FDA granted accelerated approval to the tyrosine kinase inhibitor sunvozertinib (Zegfrovy) for advanced non-small cell ...
The FDA's Dr. Vinay Prasad said that he disagreed with the agency's career vaccine reviewers about COVID shot approvals.
FDA researchers report that the upper end of reported consumer use (~400mg of daily CBD intake) of cannabidiol (CBD) may ...
The trove of more than 200 letters is part of a pledge of transparency from the agency, with the intention to increase public ...