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As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its jurisdiction. Some letters are not ...
As part of its enforcement activities, the Food and Drug Administration (FDA) sends warning letters to entities under its jurisdiction. Some letters are ...
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News-Medical.Net on MSNIndiana University researcher helps develop FDA-approved Alzheimer’s testA first-of-its-kind blood test to detect amyloid plaques in the brain associated with Alzheimer's disease recently received ...
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News-Medical.Net on MSNSolascure receives FDA Fast Track Designation for Aurase Wound Gel to treat calciphylaxis ulcersSOLASCURE Ltd (SolasCure), a biotechnology company developing a novel treatment to transform chronic wound healing, today ...
(Reuters) -The U.S. Food and Drug Administration extended the review of KalVista Pharmaceuticals' drug for a type of ...
Known as Enflonsia, the drug will compete for market share with Sanofi and AstraZeneca’s in-demand Beyfortus, which quickly ...
The outbreak has sickened 79 people across seven states, according to the Centers for Disease Control and Prevention. At ...
FDA assigns PDUFA target action date of January 31, 2026 WARREN, N.J., June 16, 2025 (GLOBE NEWSWIRE) -- Aquestive Thera ...
Health Secretary Robert F. Kennedy Jr.’s decision to revoke the Covid vaccine recommendation for pregnant women has raised ...
Rakuten Medical, Inc., a global biotechnology company developing and commercializing Alluminox™ platform-based photoimmunotherapy, today announced that it was selected by the U.S. Food and Drug ...
HADLIMA™ (adalimumab-bwwd) injection, 40 mg/0.4 mL & 40 mg/0.8 mL is now interchangeable with all high- and low-concentration presentations (autoinjector, prefilled syringe, and single-dose vial ...
The Food and Drug Administration has officially launched "Elsa," a generative artificial intelligence platform designed to ...
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