This book covers the overarching principles of GCP that are the key requirements to be followed in all clinical trials.
The principles presented in this book are reproduced from the Step 4 ICH E6(R3) guideline of January 2025.

This principles are important for everyone involved in human clinical trials whether commercial or non-commercial. 

It is especially suitable for those who do not need to know the detail of their practical implementation presented in Annex 1 and the Appendices of the E6(R3) guideline, such as administrators, coordinators and those in departments outside clinical operations.