The U.S. Food and Drug Administration said on Friday it has launched a new pilot program to speed up the review process for ...

The U.S. Food and Drug Administration has introduced a new pilot program aimed at accelerating the review process for generic drugs that are both tested and produced entirely within the United States.

To enhance retailer compliance and combat youth vaping, the FDA targets vape shops, convenience stores, and gas stations ...

Patient Investigational New Drug (sIND) applications in the United States SAN FRANCISCO, CA / ACCESS Newswire / September 30, 2025 / Jaguar Health (NASDAQ:JAGX) today announced that Jaguar family ...

The FDA has expanded its Early Alert program to give the healthcare industry earlier visibility into potential high-risk medical device issues. The agency’s Center for Devices and Radiological Health ...

New tobacco products must submit a PMTA and receive authorization, or a marketing granted order (MGO), from the FDA in order to be legally sold in the United States. In January, the FDA issued MGOs to ...

The Food and Drug Administration has launched a new transparency policy for the reporting of foodborne illness outbreak ...

Following up on previous, dimly received issuances, a new set of ideas published by the FDA to streamline regulatory pathways ...

REMS assessments found no cases of Torsades de pointes or unexplained sudden deaths among patients taking vandetanib during ...

In victory for struggling medical providers, law protecting a federal drug discount program in RI goes into effect despite ...

After a successful pilot, the agency has lifted the limitations on when it will provide early information about potentially ...