One drinking water recall issued earlier this year by the U.S. Food and Drug Administration was terminated last week.
The first fully FDA-approved at-home test kit to combine COVID-19 and flu tests is now available. It’s called the Healgen ...
Pharmacies that make customized medications are asking the federal Food and Drug Administration to protect their right to ...
A Vitamin B supplement has been recalled due to being incorrectly formulated with niacin rather than niacinamide.
The U.S. patient population for Revuforj in its approved indication is roughly 2,000 according to Syndax. KMT2A leukemias ...
Think Surgical announced today that it received FDA 510(k) clearance to use its TMINI surgical robot with the LinkSymphoKnee.
The US Food and Drug Administration (FDA) has approved Syndax Pharmaceuticals' Revuforj (revumenib) for treating relapsed or ...
The FDA-cleared Spectral CT 7500 RT, a detector-based computed tomography radiotherapy solution aimed to enhance radiation ...
Kennedy has been most vocal about the FDA, an agency that oversees nearly $3 trillion in medicines, food and tobacco products ...
The FDA has just dropped a truth bomb: if you’ve been relying on those familiar red pills for a stuffy nose, it might be time ...
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 ...