The U.S. Food and Drug Administration must quickly restore commonsense guardrails on the abortion pill to safeguard women’s health and save lives.

FDA Establishes April 23, 2026 as PDUFA Target Date for Review of Submission Seeking Approval for GTx-104 in the Treatment of Patients with aneurysmal Subarachnoid Hemorrhage (aSAH) Comprehensive Data ...

The Food and Drug Administration (FDA), an attached agency of the Department of Health, has approved the commercial use of the country’s first vaccine against bird flu, according to the Department of ...

House Bill 25, filed by state Rep. Joanne Shofner, R-Nacogdoches, would not put the drug out on pharmacy shelves. But if her ...

Two lots of Viva Raw frozen pet food for dogs and cats have been recalled for potential Salmonella and Listeria contamination ...

A fresh pet food service is voluntarily recalling some of its dog and cat food due to concerns that it could be contaminated ...

August 27, 2025Susan C. WincklerChief Executive OfficerReagan-Udall Foundation for the Food and Drug AdministrationWashington, DC 20036 Re: Public Meeting on Demand Forecasting for Controlled ...

CRISPR Therapeutics is a speculative buy for aggressive investors, driven by the commercial launch and multibillion-dollar ...

Under the leadership and guidance of Donald Trump, U.S. Health Secretary Robert Kennedy Jr. and the Republican-controlled Congress have gutted one of the most basic responsibilities of government: ...

In the following Q&A, Vrana, who is also the Elliott S. Vesell Professor of Pharmacology at the Penn State College of ...

Bayer submitted an application to the U.S.'s Food and Drug Administration to get approval for its gadoquatrane agent, a substance used to improve the quality of magnetic resonance imaging scans.

As of July 1, a critical surveillance program is monitoring for only two pathogens instead of the usual eight.