The US Food and Drug Administration aims to revoke 52 standards of identity (SOI) across a swath of food categories, claiming ...

Charleigh Pollock has a neurological disorder called Batten disease that leaves her with recurring severe seizures and ...

The culture of academic medicine needs to change, FDA Commissioner Marty Makary, MD, MPH, said at an event sponsored by The ...

Hormone therapy has endured a rather bumpy history after the Women’s Health Initiative published clinical trial data in 2002 ...

For instance, "the backlog of FOIAs ... is enormous," he said. Califf said the FDA has far greater opportunities for improved ...

As such, the FDA has classified the New Mexico Pinon Coffee pod recall as a Class III risk. The FDA defines such a risk as “a ...

After a federal ban in 2022 kneecapped the popular vape company, the Food and Drug Administration, under the watch of MAHA ...

Overview of Nanotechnology Drug Delivery MarketThe global Nanotechnology Drug Delivery Market is valued at USD 97.98 Billion ...

The team spent 14 months investigating and found that the FDA had allowed more than 150 potentially unsafe drugs in the U.S.

Capecitabine tablets build momentum for company's transparent business model; goal to create significant savings for patients, health system Potential ...

Scientists have successfully restored hearing in animal models of ENPP1 deficiency, a genetic disease in which individuals ...

The sale represents Clever Culture’s fifth engagement with a leading pharma manufacturer, including AstraZeneca, Bristol Myers Squibb and Thermo Fisher. The company is due to report its Q4 FY25 ...