NEW YORK (PIX11) — The first fully FDA-approved at-home test kit to combine COVID-19 and flu tests is now available. It’s ...
One drinking water recall issued earlier this year by the U.S. Food and Drug Administration was terminated last week.
FoundationOne Liquid CDx is now FDA-approved to identify mNSCLC patients with MET exon 14 skipping alterations for ...
The FDA is set to give its decision on SNY and REGN's sBLA for Dupixent for chronic spontaneous urticaria on April 18, 2025.
A Vitamin B supplement has been recalled due to being incorrectly formulated with niacin rather than niacinamide.
Pharmacies that make customized medications are asking the federal Food and Drug Administration to protect their right to ...
The U.S. patient population for Revuforj in its approved indication is roughly 2,000 according to Syndax. KMT2A leukemias ...
The US Food and Drug Administration (FDA) has approved Syndax Pharmaceuticals' Revuforj (revumenib) for treating relapsed or ...
Think Surgical announced today that it received FDA 510(k) clearance to use its TMINI surgical robot with the LinkSymphoKnee.
The FDA-cleared Spectral CT 7500 RT, a detector-based computed tomography radiotherapy solution aimed to enhance radiation ...
The recent approval of their lead asset, Aucatzyl, by the FDA is seen as a pivotal factor in de-risking the company’s technology platform and manufacturing capabilities. The differentiated safety ...