Review committee: accredited MREC or CCMO?
Before research with human subjects can commence in the Netherlands the research file must first be approved by an accredited MREC or the CCMO. This requires you to submit a complete research file. On the section of our website on CTR, you find information on the submission of research with a medicinal product under CTR.
In order to determine which committee should review your research, you can use the Committee Finder.
Do not forget to check the meeting dates and the submission deadlines for the committee carrying out the review (MREC or CCMO). To prevent any misunderstandings, and when in doubt over the review timelines, contact the accredited MREC or the CCMO.