The U.S. Food and Drug Administration (FDA) terminated a recall for Berkeley Club Beverages water on November 13 and recently ...
Pharmacies that make customized medications are asking the federal Food and Drug Administration to protect their right to ...
The US Food and Drug Administration (FDA) has approved Syndax Pharmaceuticals' Revuforj (revumenib) for treating relapsed or ...
A Vitamin B supplement has been recalled due to being incorrectly formulated with niacin rather than niacinamide.
Think Surgical announced today that it received FDA 510(k) clearance to use its TMINI surgical robot with the LinkSymphoKnee.
The U.S. patient population for Revuforj in its approved indication is roughly 2,000 according to Syndax. KMT2A leukemias ...
The FDA-cleared Spectral CT 7500 RT, a detector-based computed tomography radiotherapy solution aimed to enhance radiation ...
Revuforj is the first so-called menin inhibitor cleared in the U.S., securing FDA approval for use in adults and certain ...
The U.S. Food and Drug Administration ( FDA) now requires TV and radio drug ads to be clearer and more direct. The new ...
BrightHeart announced that it received FDA 510(k) clearance for its first AI software for prenatal ultrasound evaluations of ...
An FDA advisory committee has unanimously concluded that oral phenylephrine, a decongestant found in many cold and flu ...