INDIANA- On Monday, October 21, from 9 a.m. to 4:30 p.m. EDT, the U.S. Food and Drug Administration (FDA) and the National ...

FILE PHOTO: Signage is seen outside of the Food and Drug Administration (FDA) headquarters in White Oak, Maryland, U.S., August 29, 2020. REUTERS/Andrew Kelly Aug 29 (Reuters) – The U.S. Food ...

(Reuters) -The U.S. Food and Drug Administration issued warning letters to two Chinese third-party testing firms on Wednesday ...

The Food and Drug Administration is ramping up its investigation of the clinical trials that tested an Ecstasy-based therapy, after the agency earlier rejected the application for its approval.

Rezolute Inc said on Monday the U.S. Food and Drug Administration had lifted its partial clinical hold on a late-stage study ...

suicide and overdose rates (Photo by Robert Alexander/Getty Images) This is the public health reality that the FDA had to contend with when making this decision. The enormity of the PTSD crisis ...

Members of the Democratic Women’s Caucus last week urged FDA Commissioner Robert Califf to address the safety concerns.

US FDA, White Oak Building 51, Room 3184, 10903 New Hampshire Ave, Silver Spring, MD 20993-0002, USA 8 Regulatory Science Research Division, Office of Regulatory Science, Pharmaceuticals & Medical ...

The U.S. Food and Drug Administration approved Zevra Therapeutics' drug for a rare and fatal genetic disorder, the first ...

Healthcare & Pharmaceuticalscategory US FDA approves Eli Lilly's drug for eczema September 17, 2024 Healthcare & Pharmaceuticalscategory Sanofi, AstraZeneca win US approval for RSV therapy ...

Mighty Oak is a medical device development company focused on spinal surgery solutions. Medical Oak Chief Medical Officer ...

(Reuters) - The U.S. Food and Drug Administration on Thursday authorized the first over-the-counter hearing aid software ...