This e-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.