Gujarat-based Sudeep Pharma, a technology-led manufacturer of excipients and specialty ingredients for the pharmaceutical, food and nutrition industries, has filed its draft red herring prospectus ...

Alembic Pharma has received a cumulative total of 223 Abbreviated New Drug Application (ANDA) approvals (200 final approvals ...

Sun Pharma shares dropped in trade after the company announced that United States Food and Drug Administration (USFDA) has ...

Gujarat accelerates drug testing infrastructure with Rs. 8 crore funding for Rajkot lab: Shardul Nautiyal, Mumbai Thursday, June 12, 2025, 08:00 Hrs [IST] In a significant boost t ...

The US FDA conducted a good manufacturing practices inspection at the Halol facility from June 2-13, 2025, the Mumbai-based ...

Zydus Lifesciences has informed that it has received the establishment inspection report (EIR) from the U.S Food and Drug Administration (USFDA) for its active pharmaceutical ingredient (API) ...

FDA's former top official warns of "giving people false hope" after RFK Jr.'s autism claims 10:38. Food and Drug Administration officials have told some scientists and inspections staff that their ...

The U.S. Food and Drug Administration is replacing animal testing with human-relevant methods, including artificial intelligence, when developing monoclonal antibody therapies and other drugs.