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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 drugmakers, a significant move to increase transparency of the agency's work.
A growing disconnect remains between what generics are approved and what are actually accessible, GoodRx said.
US regulators approved Moderna Inc.’s Covid vaccine for children, but for a narrower group than before, continuing Robert F.
Used for diagnosing gastroesophageal reflux, the devices may not attach or detach correctly, potentially causing serious ...
Weaver Nut Company, Inc. announced a recall for specific lots of its semi-sweet chocolate nonpareils on June 17 due to the undeclared presence of milk.
In discussions with multiple potential animal health company partners to collaborate to bring Canalevia®, conditionally ...
Beyond staff cuts, the departures of some longtime investigators in recent months have left less experienced people tasked ...
WASHINGTON — The steady erosion of experienced staff at the Food and Drug Administration is slowly compromising the agency’s ...
The company had blamed FDA "resource constraints" for the delay, while a rival drug for hereditary angioedema received an ...
Spikevax is now approved for all adults aged 65 years and older, and individuals aged 6 months through 64 years at increased risk for COVID-19 disease CAMBRIDGE, MA / ACCESS Newswire / July 10, 2025 / ...
The contractor, Ajanta Caterers, had violated provisions of the Food Safety and Standards Act, 2006, and the Food Safety and ...