CDSCO Mandates SUGAM Portal for Post-Approval Changes (PAC) to Vaccine and Anti-Sera Import Licences
New Delhi: The Central Drugs Standard Control Organization (CDSCO) has issued a critical regulatory directive aimed at completely digitizing and streamlining the import and registration protocols for biological products in India.…
FDA Releases Draft Guidance To Validate Non-Animal Testing Methods (NAMs) In Drug Development
Washington: On March 18, 2026, the U.S. Food and Drug Administration (FDA) issued a draft guidance titled General Considerations for the Use of New Approach Methodologies in Drug Development.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…
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…














