This product, bioequivalent to Motegrity Tablets of Takeda Pharmaceuticals, will be manufactured at Lupin's Goa facility in ...

I know the damage misinformation and mistrust can cause. I watched as unvaccinated patients cursed COVID vaccines to my face, even as they were dying.

Science denial can be somewhat obvious, she said, such as ignoring medical advice, denying climate change or spreading ...

For example, the food additive azodicarbonamide, known as ADA and used as a bleaching agent in cereal flours, is included on ...

PathPresenter, a leading Image Management System and workflow platform for digital pathology, has received U.S. Food and Drug ...

Health and Human Services Secretary Robert F. Kennedy Jr. testified in front of the House Committee on Energy and Commerce ...

HHS Secretary Robert F. Kennedy Jr. defended his reorganization of the agency and the proposed fiscal year 2026 budget that ...

Review of foreign scientists from countries like China began even before three Chinese scientists in Michigan were caught trying to smuggle dangerous pathogens into U.S.

Curay, the top FDA drug regulator, acknowledged that much is still in flux at the agency and introduced a new deputy.

The U.S. Food and Drug Administration said on Tuesday that it is investigating reports of two deaths due to acute liver ...

The U.S. Food and Drug Administration has approved Dupixent (dupilumab) for the treatment of adult patients with bullous pemphigoid.

InspireMD shares soared after the company said federal regulators have granted premarket application approval for its CGuard Prime Carotid Stent System. The stock was up 50% at $3.72 in after-market ...