The Revised Schedule M introduces stricter and more detailed requirements for pharmaceutical premises and equipment—aimed at enhancing product quality, minimizing contamination risk, and ensuring regulatory compliance. This course is specifically designed for plant heads, engineering teams, QA/QC professionals, and regulatory personnel involved in facility design, qualification, and maintenance.

Gain clarity on layout expectations, environmental controls, material movement, HVAC standards, and equipment validation under the new guidelines. Learn how to align your manufacturing facility with modern Good Manufacturing Practices (GMP) to meet CDSCO expectations and prepare for inspections confidently.