Stay ahead in regulatory compliance with an in-depth understanding of the Revised Schedule M—India’s updated framework governing the manufacture of Active Pharmaceutical Ingredients (APIs). This course is tailored for pharma professionals, quality assurance teams, regulatory affairs personnel, and manufacturing leaders aiming to align their operations with the latest GMP (Good Manufacturing Practices) as per the revised guidelines by the Central Drugs Standard Control Organization (CDSCO).

This session will demystify the revised requirements, offer clarity on key updates, and provide actionable steps for successful implementation—ensuring your API manufacturing processes meet national and international quality standards.