This rising trend mirrors the evolution of the pharmaceutical industry in terms of investment and utilisation of novel ...

The US Food and Drug Administration announced this month that it's effectively banning Red No. 3, the controversial ...

The Food and Drug Administration has ignited a heated debate with its latest review of menthol cigarettes, revealing ...

The FDA granted priority review for belzutifan for treating advanced pheochromocytoma and paraganglioma, with a PDUFA date ...

The US Food and Drug Administration (FDA) will soon decide on whether to expand the label of MSD’s Welireg (belzutifan) to ...

The U.S. Food and Drug Administration formally authorized Zyn nicotine pouches for sale after conducting an "extensive ...

"We need to know what adverse events are. We need to understand the safety of every drug, mifepristone, and every other drug.

The NDA is supported by data from a clinical trial that compared the absorption and efficacy of the nasal treatment with oral and IV bumetanide in 68 healthy adults.

The FDA has accepted a priority review sNDA for Welireg in adults and pediatric patients with advanced or metastatic ...

Merck (MRK) announced the U.S. FDA has accepted for priority review a supplemental new drug application seeking approval of Welireg, Merck’s ...