Tidmarsh, from the FDA, assured the pro-fluoride contingent that if supplements are banned, there is still one way to get them back on the market: as a drug.

The Food and Drug Administration named a longtime pharmaceutical executive to run the agency's drug program.

NBC News medical contributor Dr. Natalie Azar reports on the FDA panel discussion of the use of antidepressants during pregnancy. The panel shared misinformation and facts taken out of context ...

The FDA has published its proposed agenda for 2025 guidance, including new topics such as food colorings. Topics on the agenda are a priority for the Food ...

PathPresenter, a leading Image Management System and workflow platform for digital pathology, has received U.S. Food and Drug Administration (FDA) 510 (k) clearance for the PathPresenter Clinical ...

KalVista Pharmaceuticals' said on Friday that the U.S. Food and Drug Administration had extended the review of its drug for a type of hereditary swelling disorder due to heavy workload and limited ...

The FDA first approved mifepristone about a quarter of a century ago, and it's proven to be safe and effective. So why is the FDA reviewing it again?

Hyperfine Announces FDA Clearance of a New Next-Generation Swoop® System Powered by Optive AI™ Software, Delivering a Transformative Leap in Image Quality This major Swoop® system scanner ...

Reuters spoke to seven biotech executives, investors, and consultants who said that the staff departures and policy changes at the FDA had prompted some firms to consider launching trials in other ...

Today, the U.S. Food and Drug Administration (FDA) and the National Institutes of Health (NIH) announced a new, joint innovative research initiative that will serve as a key element in fulfilling ...

Now, 52 percent of Americans who identify as Republicans trust the FDA to provide accurate information on vaccines, and 51 percent trust the CDC to do the same.