Quality Risk Management (QRM) is a core component of modern pharmaceutical quality systems, as emphasized by ICH Q9, Revised Schedule M, and global GMP regulations. This course provides a structured approach to identifying, evaluating, mitigating, and documenting risks throughout the product lifecycle—from development to distribution.

Designed for pharma professionals involved in quality, compliance, and manufacturing, this training covers practical tools like FMEA, HACCP, risk matrix, and root cause analysis, helping you integrate risk-based thinking into every critical process. Whether you’re preparing for audits or driving continuous improvement, this course will enhance your team’s ability to make informed, science-based decisions.