The FDA's GRAS rule revision seeks to enhance consumer safety by requiring manufacturers to notify regulators about new food ...
Over 1.2 million medical device adverse event reports were not submitted to the US Food and Drug Administration (FDA) within the deadline set by federal regulations, finds an analysis of recent data ...
some of the affected FDA positions are tied to food regulation, medical devices, and tobacco oversight. This has led to questions about how future recalls and inspections may be managed with fewer ...
Zepbound contains the same active ingredient, tirzepatide, as Mounjaro, which is also made by Lilly and is FDA-approved to treat Type 2 diabetes. Some doctors also prescribe Mounjaro "off-label" for ...
U.S. Food and Drug Administration employees reviewing Elon Musk’s brain implant company Neuralink were fired over the weekend ...
Pfizer (NYSE:PFE) has tapped Patrizia Cavazzoni, the former head of drug regulation at the FDA, as its new chief medical ...
Objective To describe the extent of late adverse event reporting by manufacturers to the US Food and Drug Administration’s (FDA) Manufacturer And User Facility Device Experience (MAUDE) database as ...
medical products, and food. He vowed to streamline drug approvals, ensure food safety, and rebuild trust in public health, emphasizing three key themes: science-based evidence, common sense ...
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