Good Clinical Practice (GCP) Refresher Course

These sessions are appropriate for all staff who are involved in any context with clinical research, in particular for those conducting a Clinical Trial of an Investigational Medicinal Product it is a regulatory requirement.

Topics include:

• Regulation Amendments
• MHRA Inspections
• Pharmacovigilance
• Standard Operating Procedures
• Trials master files
• Clinical Trials in Glasgow

This session is relevant to individuals who have had previous GCP training.