FDA Releases Draft Guidance To Validate Non-Animal Testing Methods (NAMs) In Drug Development
Washington: On March 18, 2026, the U.S. Food and Drug Administration (FDA) issued a draft guidance titled General Considerations for the Use of New Approach Methodologies in Drug Development. The…
Parliamentary Panel Recommends Decentralisation Of Approval Of All Medical Devices
New Delhi: The Parliamentary Panel on Health and Family Welfare has recommended various significant regulatory changes in the regulation of medical devices, including decentralisation of approval for all medical devices…
Department Of Commerce Organizes Chintan Shivir To Strengthen India’s Medical Devices Export Ecosystem
New Delhi: A Chintan Shivir on “Strengthening India’s Medical Devices Export Ecosystem” was organized by the Department of Commerce in collaboration with the Department of Pharmaceuticals and the Export Promotion…
Drug Diversion Epidemic Sweeps India: Absence of Track-and-Trace System, overly Codeine Allotments, and Regulatory Apathy Fuel Misuse of Narcotic Syrups and Tablets
New Delhi — A relentless surge in seizures of codeine-based cough syrups and narcotic tablets across multiple states over the past 48-72 hours has laid bare the rampant diversion of…















