The Revised Schedule M has brought critical updates to the Good Manufacturing Practices (GMP) governing the manufacture of oral liquid pharmaceuticals, including syrups, suspensions, and solutions. This course is tailored for professionals involved in formulation, manufacturing, quality, and regulatory functions who want to ensure their oral liquid production lines are compliant with the latest standards issued by the CDSCO.

Gain a deep understanding of new infrastructure requirements, documentation protocols, water system management, cleaning validations, and contamination controls that are essential for high-quality oral liquid production. Stay audit-ready and avoid regulatory non-compliance with a step-by-step breakdown of what’s changed and how to adapt your facilities and processes accordingly.