Scott Gottlieb and Luciana Borio, a former director for medical and biodefense preparedness policy at the National Security Council, wrote a Friday op-ed in the Washington Post outlining growing concerns for the White House’s approach to eliminating bird flu mutations.

As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its jurisdiction. Some letters are not

The impacted products have now been given a Class I risk classification by the U.S. Food and Drug Administration.

Produce supplier Braga Fresh has issued a ‘precautionary advisory’ about the product, which is no longer in stores but might still be in people’s freezers. The U.S. Food and Drug Administration (FDA) is alerting the public via its recall website about a voluntary advisory issued by Braga Fresh for a batch of Marketside Broccoli Florets sold at Walmart stores across 20 states.

A discussion of the development of consumer protection law in the US through the enactment of key legislation and formation of the Food and Drug Administration (FDA).

On December 20, 2024, the FDA granted accelerated approval to the combination of encorafenib (Braftovi), cetuximab (Erbitux), and mFOLFOX6 (fluorouracil, leucovorin, and oxaliplatin) in metastatic colorectal cancer with a BRAF V600E mutation, as detected by an FDA-approved test.

This may start to bring down the cost of brand-name competitors—here's who might get access, and one major difference from the pricier kind.

Eli Lilly is seeking to end a lawsuit filed by a pharmacy trade group against the Food and Drug Administration (FDA) by joining as a defendant, stating it wants to end the

The Food and Drug Administration (FDA) will begin collecting samples of raw cow’s milk cheese from across the U.S. to test for the presence of bird flu, spurred on by the ongoing outbreaks

After plugging billions into its manufacturing network to meet rampant demand for Mounjaro and Zepbound, Eli Lilly is looking to protect its investment by wading into a lawsuit that seeks to allow | After plugging $23 billion into its manufacturing network to meet rampant demand for Mounjaro and Zepbound,

Olympus advised providers to stop using an endoscope accessory due to an infection risk linked to 120 injuries and one death.

Tislelizumab-jsgr (Tevimbra) was approved in combination with chemotherapy for the treatment of unresectable or metastatic HER2-negative (HER–) gastric or gastroesophageal junction adenocarcinoma (G/GEJ) in adults whose tumors express PD-L1.