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The U.S. Food and Drug Administration extended the review of KalVista Pharmaceuticals' drug for a type of hereditary swelling ...
(Reuters) -The U.S. Food and Drug Administration on Thursday expanded the use of Moderna's respiratory syncytial virus ...
Expanded indication builds on existing U.S. FDA approval of mRESVIA for adults aged 60 and older CAMBRIDGE, MA / ACCESS ...
THE US Food and Drug Administration (US FDA) officially approved Nutriasia's petition to remove Mang Tomas All Purpose Sauce, ...
A new article in the Journal of the American Medical Association said the FDA will implement AI into multiple processes.
Leaders of the FDA have published a list of new priorities for the agency. They want to deliver rapidly-approved cures and ...
The U.S. Food and Drug Administration expanded its approval of Moderna's respiratory syncytial virus (RSV) vaccine on ...
The FDA plans to "unleash AI" on new drug evaluations in order to "radically increase efficiency in the review process." ...
The facility can continue selling approved drugs and will also receive approvals for new filings. Shares of Syngene ...
A voluntary recall has been initiated for Dr. Pepper Zero Sugar cans across Florida, Georgia, and South Carolina after it was ...
While it is not the most common allergy in the country, almost 2 million Americans have an allergy to soy, according to Food ...
This story is from the next print edition of MIT Technology Review, which explores power—who has it, and who wants it. It’s ...