News

Police across Europe have dismantled a dark web drug marketplace known as 'Archetyp Market', the pan-European Europol police ...
KalVista Pharmaceuticals' said on Friday that the U.S. Food and Drug Administration had extended the review of its drug for a ...
Expanded indication builds on existing U.S. FDA approval of mRESVIA for adults aged 60 and older CAMBRIDGE, MA / ACCESS ...
The U.S. Food and Drug Administration on Thursday approved UroGen Pharma's drug to treat a type of bladder cancer, providing ...
The global watchdog of doping in sports says it will urge public authorities to shut down the drug-fueled Enhanced Games ...
Attorneys said many questions remain about LDT regulation after the FDA lost its legal fight. A recent warning letter could ...
Health officials want you to think twice before buying brightly colored energy shots and supplements often sold at gas ...
Sun Pharma bagged eight observations from the US-based regulatory agency US FDA, following an observation at its Halol plant ...
Leaders of the FDA have published a list of new priorities for the agency. They want to deliver rapidly-approved cures and ...
On June 10, 2025, the Commissioner of the FDA, Dr. Martin Makary, and Dr. Vinayak Prasad, the Director of the FDA’s Center for Biologics Evaluation and Research, published an article in ...
While some compounding pharmacies have stopped making alternatives to Wegovy and Zepbound since shortages were declared over, ...
The FDA plans to "unleash AI" on new drug evaluations in order to "radically increase efficiency in the review process." ...