ICH GCP (R2) Book

This pocket-sized ICH GCP booklet includes the full ICH GCP Guideline, including the latest update (Addendum R2). It is ideal for researchers, monitors, auditors, members of ethics committees and others who would like to have the Good Clinical Practice guidelines at hand.


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The pocket-size GCP booklet contains the guidelines for Good Clinical Practice (GCP) applicable to clinical (drug) research worldwide.

In this booklet, you’ll find the full content of ICH-GCP, including:

  • the responsibilities of the Medical Ethical Review Committee (METC)
  • researchers (and supervisors)
  • and sponsors in clinical trials

It also includes information about what must be included in the clinical trial protocol, the investigator’s brochure (product information), and other essential documents needed for the setup, conduct, and close-out of clinical research.

Take your GCP knowledge everywhere, with this pocket-size GCP booklet!





Learn anytime, anywhere

Learn at your own pace on your smartphone, tablet or desktop. You will have one year of access to the training and resources so you can look up information even after you’ve completed the course.

Learn Continiously

Continuous Learning can both improve clinical research quality and ensure a motivated research team. You’ll benefit from better knowledge retention and reduced risks. We When a regulatory update is announced, we update the training modules and notify you, so that you can take the updated module and earn a new GCP certificate.

Earn your gcp certificate

With our courses, you can earn and maintain your vital industry-recognized certificate. In your GCP Passport, you can now see exactly which version of a training module you were most recently trained on. This documentation in combination with the changelog will inform auditors, managers, and inspectors of the associate’s compliance with current regulations.


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