Introduction to Good Clinical Practice (GCP)

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

Topics include:

• History of Clinical Trials and the development of GCP
• Deciding what is a clinical trial
• Informed consent
• Responsibility of Research Personnel
• Pharmacovigilance
• Monitoring

This session is relevant to individuals who have no previous GCP training