The review system in the Netherlands Research covered by the Medical Research Involving Human Subjects Act and/or the Embryos Act must be submitted to an accredited Medical Research Ethics Committee (aMREC) for approval before it is carried out. In some cases, the CCMO acts as the Research Committee...
Step-by-step plan RC review Follow the step-by-step plan for research committees (RC) to find out whether your study has to be reviewed, by which committee, and what will be examined during (and after) the review itself.
Step-by-step plan CA review Follow the step-by-step plan competent authority (CA) to find out whether your study is with medicinal products and if so, which (extra) committee must give the decision whether there are 'grounds of non-acceptance' concerning the study, and what procedure must be followed before and after the review CA.
Research file and forms This page contains all the forms that may be relevant during or after the medical ethics review.
Web portal ToetsingOnline Internet portal for submission and review of medical ethics research with human subjects in the Netherlands.
