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Expert WMO GCP Course for Clinical Trials in the Netherlands

This course was previously called “Online WMO-GCP training”. Learn everything you need to know to master ICH GCP and Dutch legislation (WMO) applicable to clinical trials in the Netherlands via this highly interactive, self-paced, and certified WMO/GCP e-learning course. Includes 7 interactive modules.


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  • ICH GCP and ICH GCP R2 Addendum
  • EU Directives (2001 and 2005)
  • Dutch legislation: Medical Research Involving Human Subjects Act (WMO), WGBO and Wet BIG
  • Roles in clinical research
  • Privacy in clinical research (GDPR)
  • Informing research participants
  • Essential documents
  • Review by the Ethics Committee
  • Safety reports and safety of your subjects, incl. AEs, SAEs, and SUSARs
  • Quality management
  • Amendments and derogations
  • Final report
  • Audits and inspections



The expert course to GCP in the Netherlands is the self-paced online training solution for researchers, pharma professionals, and research staff who conduct clinical trials in the Netherlands, and need to be aware of the Good Clinical Practice guidelines, EU laws, and the Medical Research Involving Human Subjects Act (WMO) applicable to clinical research with human subjects. It is the best choice for those who like the flexibility of online learning at their own pace and time. This course translates the regulatory framework to practice and gives you the tools to directly implement the knowledge in your daily practice.

  • Transcelerate acknowledged WMO/GCP certificate
  • Efficient and interactive learning
  • Easy accessible via smartphone, tablet, or desktop
  • Self-paced and modular
  • Accredited by PE-online quality registers

The course consists of 7 online training modules in a logical order: from the design to close-out of a clinical trial. It represents a total workload of 8 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, ICH GCP E6 Addendum R2, EU Directives 2001 and 2005, the EU Privacy law, Medical Research Involving Human Subjects Act (WMO), WGBO and Wet BIG.

After you have completed all components of the GCP e-learning course for clinical trials in the Netherlands you will receive a WMO/GCP Certificate, recognized by Transcelerate and accredited by many quality registers.

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.



Module: Introduction

Module: Design
Module: Preparation
Module: Submission
Module: Start
Module: Conduct
Module: Archive (Close-out)

Module: Knowledge Test

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.

1 review for Expert WMO GCP Course for Clinical Trials in the Netherlands

  1. Published

    Amazing training that I use every day in my work!

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