This professionally developed Good Laboratory Practice (GLP) training course provides a comprehensive understanding of the regulatory requirements and operational standards governing non-clinical laboratory studies. Designed for laboratory professionals, QA personnel, and research managers, the course delivers essential knowledge to ensure robust GLP compliance aligned with international expectations.
Participants will explore the principles and global framework of OECD GLP, including the roles and responsibilities within compliant organisations, facility and equipment standards, and the implementation of Standard Operating Procedures (SOPs). The course also addresses quality assurance processes, audit preparedness, data integrity, risk management, and ethical considerations, with dedicated focus on the integration of IT systems in laboratory environments.
Updated for 2025, the course incorporates both the latest OECD position paper on IT security and the new OECD paper on quality in GLP studies, reflecting the increasing emphasis on digital integrity and continuous quality oversight in non-clinical research settings.
Learning objectives
- Understand the regulatory foundations and global expectations of GLP, including OECD principles and their application to non-clinical laboratory studies.
- Apply key components of GLP compliance in practice, including roles and responsibilities, SOPs, data integrity, quality assurance, and risk management.
- Interpret and implement current guidance on digital systems and quality oversight, including the latest OECD papers on IT security and quality in GLP environments.
Download Course Summary Leaflet
Click the link above to explore the complete course content in our PDF leaflet.
