EU CTR Foundation in the Netherlands

Our EU CTR Foundation in the Netherlands e-learning course teaches you the essentials of the European Clinical Trial Regulation and the impact on Clinical Drug trials in the Netherlands. Includes 1 interactive module, 1 test and takes 1.5 hours to complete.


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Category: Tag:


  • Principles of EU CTR (EU Clinical Trial Regulation)
  • Critical timelines for submission and review of a dossier
  • Transition period and expected implementation
  • Impact on the conduct of a clinical drug trial in the Netherlands



EU CTR stands for European Clinical Trial Regulation. The EU CTR regulation will affect everyone involved in clinical drug research in Europe and will help improve collaboration between all parties involved.

The EU CTR Foundation in the Netherlands explains the principles of the regulation, clarifies the critical timelines, helps you understand the changes, and be prepared to be EU CTR ready.

  • 1.5 hours
  • 1 Learning module
  • Online EU CTR certificate
  • Knowledge test
  • Available on desktop, smartphone or tablet
  • Accredited by several quality registers

It is an ideal introductory course suitable for anyone (clinical and non-clinical) involved or interested in medical science and drug research. The course enables you to get a good overview of the new regulations and the consequences of the implementation of clinical drug research. It is perfect for: doctors, research nurses, patients, students (medicine or biology), clinical trial assistants, employees of CROs, employees of (hospital) pharmacies.

The online course takes 1.5 hours and consists of the basic EU CTR module and a knowledge test. After completion, you will receive an online EU CTR certificate.



Module: Introduction

You’ll learn the following in this module:

  • The goal and high-level contents of the EU CTR
  • Scope of the EU CTR: to which type of research the EU CTR is applicable
  • Dutch ambition regarding the introduction of the EU CTR
  • Opportunities, benefits, and challenges of the EU CTR and submissions via the EU-portal (CTIS)
  • Information about the transitional period from CTD to EU CTR
  • Timelines of the submission- and review process according to the EU CTR regulation
  • Differences in the submission of a national trial and an international trial
  • Results of the validation phase, Assessment Part I and assessment Part II

Module: Knowledge Test

The knowledge test includes:

  • 10 questions
  • Available in English and Dutch
  • Feedback per question (afterwards)
  • 3 attempts
  • Online certificate with a score of 80 or higher

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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