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Fundamental WMO GCP Course to Start and Conduct Clinical Trials in the Netherlands

This course was previously called “Light PLUS WMO-GCP training”. Learn about basic Good Clinical Practice principles and get a detailed understanding of the knowledge required to start and conduct clinical trials in the Netherlands via this highly interactive, self-paced, and certified WMO/GCP e-learning course. Includes 3 interactive modules.


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  • Principles of ICH GCP and the ICH GCP Addendum R2
  • EU Directives 2001 & 2005
  • Dutch legislation: Medical Research Involving Human Subjects Act (WMO), WGBO, and Wet BIG
  • Privacy in clinical trials
  • Roles in clinical research
  • Recruiting and informing test subjects
  • Informed consent and privacy of data
  • Requirements for research with vulnerable subjects
  • Document and data management in research
  • Monitoring and safety of test subjects
  • Progress reports



The Fundamental WMO GCP course is the ideal foundation for Good Clinical Practice (GCP), and starting and conducting clinical trials in the Netherlands. It gives you the tools you need to start your trial, recruit and inform your subjects, adhere to the requirements for research with vulnerable subjects, ensure the privacy of data, to deal with amendments, deviations, and changes in protocol and research, adding new research locations and researchers, ensure a high level of quality and risk management, and have all safety measurements and reports in place.

This course is specifically tailored to the Dutch regulatory (WMO) framework and helps anyone involved in the start and conduct phase of clinical trials in the Netherlands. It is an ideal fundamental course for students, research coordinators, investigators, clinical trial site staff, and research nurses.

  • Efficient and interactive online learning
  • Easy accessible via smartphone, tablet or desktop
  • Self-paced and modular

The course consists of 3 online training modules: Introduction, Start, and Conduct 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 clinical trials in the Netherlands, including the Declaration of Helsinki, ICH GCP E6 Addendum R2, the EU Directives, and the WMO. If you require additional knowledge for the execution of other phases of the trial, you can easily add these modules by upgrading to an Expert online WMO GCP training package.

After you have completed all components of the Fundamental WMO/GCP e-learning course, you will receive a Certificate.

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

You’ll learn the following in this module:

  • Introduction to medical research
  • Types of clinical research (interventional, therapeutic, multi/single center)
  • History of legislation and regulations clinical research (Code of Nuremberg, Declaration of Helsinki)
  • The principles of ICH GCP incl. R2 Addendum
  • Laws and regulation clinical research Europe (EU directives 2001 and 2005, EU Regulation 536/2014)
  • Legal framework for clinical research in the Netherlands (WMO, WGBO, Wet BIG, AVG) and scope
  • The roles in clinical research: sponsor, METC, competent authority CCMO or Ministry of Health (VWS), monitor, auditor, researcher, research professional
  • Additional requirements for clinical trials of a medicinal product
  • Phases of a clinical trial of a medicinal product
  • Abbreviations and terminology in medical scientific research

Module: Start

You’ll learn the following in this module:

  • Delegate tasks and Initiation Visit
  • Supply, storage, and use of the investigational product in a trial
  • Recruitment of subjects
  • Informing subjects
  • Informed Consent procedure
  • Randomization and coding
  • Privacy of data (AVG)
  • Requirements for research with vulnerable subjects

Module: Conduct

You’ll learn the following in this module:

  • Amendments, deviations, and changes in protocol and trial
  • Adding new research sites and investigators
  • Safety reports (AE / SAE / SUSAR)
  • Safety subjects medical care and DSMB
  • Documentation and data management (source, CRF, database)
  • Monitoring/ Auditing/ Inspection
  • Quality assurance and risk management (R2 Addendum)
  • Progress reports

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 Fundamental WMO GCP Course to Start and Conduct Clinical Trials in the Netherlands

  1. matyas@igina.net

    Need to explain more so that we can clearly answer questions

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