In the first five months of 2025, 305 samples of a wide range of drugs – including lifesaving medication – drawn from ...

U.S. Food and Drug Administration. June 2024. 2 Approval letter for HADLIMA (adalimumab-bwwd) supplemental biologics license applications 761059/S-025 and 761059/S-026. U.S. Food and Drug ...

Bi, 69, served as the chief of the China Food and Drug Administration from 2015 to 2018, when he introduced regulatory overhauls that spurred innovation in China’s pharmaceutical sector.

Maharashtra’s Food and Drug Administration (FDA) has cancelled the food business licence of Zepto’s Dharavi facility after an inspection revealed multiple hygiene and food safety norms violations.

Savara Receives Refusal to File (RTF) Letter From the U.S. Food and Drug Administration (FDA) for the Biologics License Application (BLA) for MOLBREEVI* to Treat Patients With Autoimmune Pulmonary ...

Domestic equity benchmarks surged more than one per cent on Friday amid broad-based buying, with financial, energy, IT and ...

Gynecologic cancer (Gyn-Ca) treatment has seen meaningful advancements in therapeutic outcomes in the past decade with the introduction of new therapies. 1-4 Despite this progress, not all populations ...

MUMBAI: The Maharashtra Food and Drug Administration (FDA) has suspended the food business license of Kiranakart Technologies Pvt. Ltd.—the parent company of quick-commerce platform Zepto—for ...

Maharashtra Food and Drug Administration (FDA) has suspended Zepto's Dharavi warehouse licencedue to non-compliance with food safety standards.

Former FDA commissioner on the Trump administration’s troubled decision to cut staff who were going to help create generic GLP-1s.

The U.S. Food and Drug Administration (FDA) has issued a warning letter to Eden F&C Co. Ltd, a seafood processing facility located at 6381 Nambu-Ro, Naebung-Myeon, Boeun-gun, Chungcheongbuk-do ...