This comprehensive online GMP training course is designed for anyone working in pharmaceutical manufacturing, quality, laboratory, engineering, or clinical trial supply settings. Whether you’re new to the industry or looking for a practical refresher, this course will strengthen your understanding of GMP principles, regulatory expectations, and real-world application.
Covering core GMP topics including quality systems, documentation, hygiene, production, warehousing, and distribution, the course also explores the role of GMP in laboratories, engineering, and trial sites — providing a functional, cross-departmental perspective.
Aligned with the latest global regulations and guidance, including ICH E6(R3) and updates to Good Distribution Practice (GDP), this training ensures you stay current with the evolving expectations of regulators and inspectors.
By the end of the course, learners will have a firm grasp of GMP essentials and the confidence to apply them in their specific roles — helping support product quality, patient safety, and compliance.
Learning objectives
- Understand the foundational principles of Good Manufacturing Practice (GMP) and their role in ensuring product quality, regulatory compliance, and patient safety across the pharmaceutical lifecycle.
- Identify and apply GMP requirements relevant to key operational areas, including manufacturing, laboratories, engineering, warehousing, and clinical trial sites.
- Interpret and implement current GMP regulations and guidance, including recent updates from ICH E6(R3) and Good Distribution Practice (GDP), within day-to-day responsibilities.
Download Course Summary Leaflet
Click the link above to explore the complete course content in our PDF leaflet.
