Discover the essentials of Good Clinical Practice (GCP) and why they matter – even if you’re not directly involved in trial operations.

Administrators, assistants, documentation specialists and other non-technical staff have a very important role to play in clinical trials.

Whilst they might not need to know GCP in all its detail, they should be aware of the principles that facilitate participant protection, the collection

and reporting of reliable clinical trial data and the maintenance of essential records.

This short guide takes you through the key principles of GCP and explains how your support contributes to participant protection and the recording of reliable

results. By reading this guide you should be better equipped with the knowledge required to play your part in helping to ensure compliance with GCP.

Author:  Prof Dr David Hutchinson