A voluntary recall has been initiated for Dr. Pepper Zero Sugar cans across Florida, Georgia, and South Carolina after it was ...

Tennessee enacts 177 new laws, covering areas from school vouchers to women's health. NASHVILLE, Tenn. — Starting July 1, 177 ...

As the use of medical device software and software as a medical device (SaMD) grows, regulatory bodies around the world are ...

What we set out to do, and what we’ve continued working on, is exploring all the ways we could create the best possible ...

The FDA is introducing a new priority voucher program designed to shorten the drug review process from 10 to 12 months down to one or two months, according to the agency. | The FDA is introducing a ...

Concerns over food safety have resurfaced following a major product recall involving a well-known organic snack brand. The ...

The FDA’s Breakthrough Device program is reserved for technologies that may significantly improve outcomes for patients with life-threatening or irreversibly debilitating conditions. It offers ...

A device that is a noninvasive, drug-free way to treat and prevent migraine headaches is now FDA-approved for use in children. Millions of people suffer from migraine headaches that can be ...

June 03, 2025--(BUSINESS WIRE)--Guardant Health, Inc. (Nasdaq: GH), a leading precision oncology company, today announced that its Shield multi-cancer detection (MCD) test has been granted ...

DAVENPORT, Iowa (KWQC) - The Food and Drug Administration recently approved Journavx to treat short-term pain. It’s a new class of non-opioid pain medication for treating adults and the first ...