The expert course to ICH GCP for Sites is the self-paced online training solution for clinical research professionals who lead and conduct international clinical trials in sites in ICH regions, and need to be aware of the sites responsibilities as laid down in Chapter 4 of the Good Clinical Practice guideline applicable to clinical research with human subjects. 

• 4 hours
• 6 modules (Introduction, trial setup, preparation, submission, conduct and close-out)
• Knowledge test with 25 questions and 3 attempts
• Available in English
• Transcelerate acknowledged
• Acknowledged GCP certificate
• Foccused on International clinical research from a sites perspective
• Efficient and interactive learning
• Easy accessible via smartphone, tablet or desktop
• Self-paced and modular

The course consists of 6 online training modules in a logical order: from the design to close-out of a clinical trial. It represents a total workload of 4 hours. The modules are divided into chapters of 10 minutes and consist of the guidelines which apply to international clinical trials, including the Declaration of Helsinki, and ICH GCP E6 Addendum R2.

After you have completed all components of the ICH GCP elearning course, you will receive a GCP Certificate.  This course complements the Expert ICH GCP for Sponsors which fulfil requirements for the mutual recognition of GCP training. All training courses include one-year access to the online training. With our continuous learning model, we will keep you up-to-date with changing regulations and guidelines. 

Enroll now to get started with the online learning modules on your smartphone, tablet or desktop computer!