Regulatory Courses

This one-day course is co-developed and given by the Belgian Competent Authorities. European legislation is one thing; the practical implementation in Belgian is something else.

The programme has been revised to capture the most recent developments related to the implementation of the EU Clinical Trial Regulation 536/2014 and focuses on the current and future legal requirements of performing clinical trials with medicinal products in Belgium.
The Belgian law of 7 May 2004 on experiments on humans implements the European directive 2001/20/EC. A number of Royal Decrees and circular letters have been published, which detail the practical implementation of the law. This training helps participants understand how the currently valid Belgian legal rules should be applied. A separate part of the training is dedicated to the European Clinical Trial Regulation 536/2014, which will repeal directive 2001/20/EC after a transition phase. Important information relating to steps under development for implementation in Belgium will be presented.


Course time
09h00 - 17h00
Who should attend

Everyone involved in clinical research, including: Pharmaceutical companies, Contract Research Organisations (CROs), Investigators, Site Personnel and Ethics Committee Members.

People from clinical operations, regulatory affairs, quality assurance and pharmacovigilance departments within the pharmaceutical industry

Programme highlights
  • Overview of current European and Belgian Legislation concerning Clinical Trials (incl. Amendments & Safety Reporting)
  • Clinical Trials and the Belgian Ethics Committees
  • The European Clinical Trial Regulation 536/2014 in short
  • Update on the implementation of the EU Clinical Trial Regulation 536/2014
  • Current Clinical Trial Requirements by the Belgian Competent Authority from first hand
Learning Objectives
  • Getting an overview of the implementation of the EU directive into Belgian law
  • Detailling the practical implementation, illustrated with examples
  • Understanding all Belgian laws related to Clinical Research
  • Having an update on the latest status on the implementation of the EU Clinical Trial Regulation 536

Book a course

Date Lang Location
Proceeding your application may take up to 24 working hours. In case of question, contact
950,00 € excl. VAT (if applicable)


Gerda Sabbe
May 2010
Medical Device Works

I would like to thank the trainers of ECCRT with the course:  “EU Clinical Trial Directive: implementation in Belgium”.   Even though my current interest is mostly in “medical devices”, I learned a great deal from both Mr. Bonnarens and Dr. Verbeeck.  The information was presented very well, even though the materials can, in itself, be quite boring. In addition the practical handling of the subscription, reception, training, breaks and conclusion of the meeting went smoothly:  congratulations.