Good Clinical Practice (GCP) is an international ethical and scientific quality standard for the conduct of trials involving human participants. GCP training is essential for anyone involved in the conduct of clinical trials. It ensures that clinical trial professionals understand their responsibilities and are well-equipped to protect participant rights, ensure participant safety, and generate reliable trial data.
The guideline for GCP, published by the International Council for Harmonisation (ICH) as ‘ICH E6’, has undergone a major renovation. The final version of the updated guidance (ICH E6(R3)) was adopted in January 2025.
As a provider of ICH GCP training, Genesis Research Services has been preparing for this update since the initial draft was released in 2023. We are now proud to announce the release of our new Good Clinical Practice (ICH GCP (R3)) Online Training Course.
What’s covered in the new course?
Key topics covered in the new course include:
1. Overview of Good Clinical Practice
2. What’s New in ICH E6(R3)?
3. The Principles of ICH GCP (R3)
4. Clinical Trial Roles – An Overview
5. Roles & Responsibilities
§ Sponsor
§ Investigator
§ Ethics Committee
6. Informed Consent of Trial Participants
7. Trial Records & Data Governance
8. Trial Conduct & Management
What has changed?
u Redesigned, restructured, and streamlined content.
u Engaging learning tools – including mini quizzes and interactive questions.
u New and expanded topics – including Data Governance and Protocol Development.
u Downloadable resources – including a fully study guide and summary sheets.
What will happen to the old course?
Our old GCP course, which covered ICH E6(R2), can no longer be purchased. Enrolled users will still be able to access the course for another 12 months to complete training and download their certificate.
New users and those requiring GCP recertification can purchase the new course.








