Revised Schedule - M

REVISED SCHEDULE-M

The technical and techno-legal experts possessing 20 to 30 years of experience in implementing stringent pharmaceutical regulatory norms/requirements shall facilitate and liaise with your organisation for implementing the requirements as per new revised Schedule-M, notified by CDSCO on 28-12-2023, in a time bound manner.

The project involves the following elements;

1. Setting up a robust Quality Management System for the organisation.
2. Documentation system based on national and international standards covering entire aspects of revised Schedule-M.
3. Validation of equipment, Machineries and Process.
4. Training of staff/employees on Revised Schedule-M and pathway for implementation.
5. Performing/conducting Audits and monitoring the implementation of Revised Schedule-M.