With the implementation of the Revised Schedule M, regulatory expectations for sterile pharmaceutical manufacturing have become more stringent—especially around validation of sterilisers and aseptic processing. This course is specially designed for professionals working in sterile manufacturing environments who need to ensure full compliance with the updated GMP norms issued by CDSCO.

Learn how to effectively validate autoclaves, dry heat sterilisers, and aseptic filling processes as per current regulatory standards. Discover risk-based approaches to process validation, media fills, and environmental monitoring that meet both national and international guidelines.

This training session delivers a practical, compliance-focused guide to mastering the critical aspects of sterility assurance, ensuring you stay inspection-ready and aligned with the latest pharma manufacturing expectations.