News

AbbVie has received accelerated approval from the U.S. Food and Drug Administration (FDA) for EMRELIS (telisotuzumab ...
The FDA is seeking public input on Operation Stork Speed, a review of and effort to improve the quality of infant formula.
Amidst policy shifts and layoffs at the FDA, some biotechs are considering moving early clinical trials to Europe or ...
In-N-Out Burger is removing artificial dyes from shakes and lemonade, aligning with the FDA's ban on synthetic dyes. The ...
The U.S. Food and Drug Administration (FDA) on Wednesday approved Merck & Co. Inc.’s (NYSE:MRK) Welireg (belzutifan) for ...
BioCardia, Inc. ( NASDAQ: BCDA) Q1 2025 Earnings Conference Call May 14, 2025, 16:30 PM ET Peter Altman - President and CEO David McClung - CFO Miranda Peto - IR Joe Pantginis - H.C. Wainwright Laura ...
President Donald Trump signed an Executive Order (EO) titled “Delivering Most-Favored-Nation Prescription Drug Pricing to American Patients” aimed ...
Health and Human Services Secretary Robert F. Kennedy Jr. said Wednesday the Food and Drug Administration should change the ...
Merck has received approval from the Food and Drug Administration for Welireg, its oral inhibitor for patients with certain rare types of neuroendocrine tumors. The company said Wednesday the ...
The test detects the MET protein that is over-expressed in some patients with non-squamous non-small cell lung cancer.
Monogram Technologies has received clearance from the Food and Drug Administration for its mBôs Total Knee Arthroplasty system. The company said Wednesday the clearance means it can start marketing ...
The PAM Health Rehabilitation of Tulsa held free mini screenings to show stroke survivors a new FDA-approved rehabilitation ...