With the rollout of the Revised Schedule M, the expectations around materials management, vendor qualification, and reference standards in pharmaceutical manufacturing have been significantly upgraded. This course is designed to help pharma professionals ensure full GMP compliance in these critical areas—essential for maintaining product quality, regulatory readiness, and supply chain integrity.

Through this focused training, you will learn how to align your raw material sourcing, supplier evaluation, and reference standard handling with the latest CDSCO regulations and international quality benchmarks. Gain clarity on documentation, testing, audits, and risk-based qualification processes that are now mandatory under the revised guidelines.

Whether you’re in quality assurance, procurement, or regulatory affairs, this session will give you actionable insights to tighten controls, reduce compliance risks, and prepare for successful inspections.