Good Clinical Practice (GCP) for Labs
Audience: Member of University - ALL Format: In PersonPrinciples of Good Clinical Practice (GCP) for staff working in laboratories handling samples derived in clinical trials
Wednesday, 15 July 2026, 12.30pm to 4.30pm
Laboratories handling samples derived from Clinical Trials of Investigational Medicinal Products (CTIMPs) are legally obliged to adhere to Good Clinical Practice (GCP). But what does this mean in practice?
This course will provide a brief overview of CTIMP design and delivery, then guide you through the principles of GCP and what this means from the perspective of the laboratory. Key areas covered include:
>Requirements of a Quality Management System
>Roles and responsibilities
>Participant consent
>Ensuring data integrity
>Managing errors, deviations and incidents
>Archiving
>MHRA inspections
Email rgea.training@admin.ox.ac.uk to book this session date.
Department: Medical Sciences (Division)
Organiser: Research Governance, Ethics & Assurance (RGEA) Training
Host: Training provided by Research Governance, Ethics & Assurance