With the updated Revised Schedule M, the importance of self-inspection and internal quality audits has been significantly elevated to ensure continuous compliance and improvement. This course is tailored to equip pharmaceutical professionals with the knowledge and tools required to design, execute, and document robust self-inspection programs aligned with GMP and regulatory expectations.

Participants will learn how to proactively identify gaps, implement corrective and preventive actions (CAPA), and drive a culture of quality ownership and regulatory readiness across departments.