Many critical functions of the food division of the Food and Drug Administration have been drastically slowed or entirely stopped since late January, potentially making Americans less safe ...

A pair of Democratic senators are pushing back against the Trump administration’s decision to terminate a host of positions at the Food and Drug Administration, raising concerns that the firings ...

NS Pharma, a subsidiary of Nippon Shinyaku Co., announced that acceptance has been received by Capricor Therapeutics (CAPR) from the U.S. FDA for the Biologics License Application filing for ...

The U.S. Food and Drug Administration has made an update to its MadeGood granola bar recall. The popular granola bars, sold on Amazon and in stores like Target, Whole Foods, Wegmans, CVS ...

Capricor Therapeutics (CAPR) announced the U.S. Food and Drug Administration has accepted for review its Biologics License Application seeking full approval for deramiocel, an investigational cell ...

The Food and Drug Administration uses import alerts to enforce U.S. food safety regulations for food from foreign countries. The agency updates and modifies the alerts as needed. Recent ...

The Food and Drug Administration (FDA) oversees manufacturers of infant formulas and helps ensure that these products are safe and support healthy growth in infants who consume them. The FDA ...

A U.S. Food and Drug Administration building is seen behind FDA logos at a bus stop on the agency's campus in Silver Spring, Md., on Aug. 2, 2018. A U.S. Food and Drug Administration building is ...

MEDVi, a cutting-edge telehealth weight loss program, aims to simplify and enhance weight management through FDA-approved GLP-1 medications. With a science-backed approach, MEDVi offers ...

Shea, one of 1,310 people who responded to a poll the health policy research group KFF conducted on health care priorities, said he assumes the FDA is making sure the ingredients are safe.

The picture gets bleaker for iconic film company Technicolor with updates that Technicolor Creative Studios UK Limited is due to file for administration today [Monday 24 February] and multiple ...

Sanofi has won FDA approval for its sutimlimab for cold agglutinin disease (CAD) at the second time of asking, becoming the first approved therapy for the rare blood disorder in the US.