The federal government's investigation into a recall of Salmonella-contaminated brown cage-free and certified-organic eggs ...

The Food and Drug Administration uses import alerts to enforce U.S. food safety regulations for food from foreign countries. The agency updates and ...

The Food and Drug Administration (FDA) granted full approval on Thursday to Moderna’s COVID-19 vaccine for children, making it the first COVID shot for kids aged 6 months to 11 years old that is ...

Beyond staff cuts, the departures of some longtime investigators in recent months have left less experienced people tasked ...

To mark his first 100 days as head of the FDA, Martin Makary is touting his efforts to change the agency’s operations. The Food and Drug Administration ...

In discussions with multiple potential animal health company partners to collaborate to bring Canalevia®, conditionally ...

The company expects to make the updated Spikevax available to U.S. patients in time for the 2025-26 respiratory virus season.

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.

The FDA published more than 200 letters that it sent to companies when it rejected their medicines, but the letters came with a caveat.

KalVista Pharmaceuticals said on Monday the U.S. Food and Drug Administration has approved its drug, the first on-demand oral treatment for a type of hereditary swelling disorder, sending its shares ...

The U.S. Food and Drug Administration updated its blood donation guidelines. Now, it goes off individual risk assessment ...