Medical Research Ethics Committee (MREC) Utrecht
Medical Research Ethics Committee (MREC) Utrecht
On this website you will find information about the submission of a research file to the MREC Utrecht, about the Medical Research Involving Human Subjects Act (WMO), and about related matters.
Average review period of the MREC Utrecht in 2019:
- Files for research with a medicinal product (n=31):
48 days (statutory maximum: 60 days) - Files for other types of research (n=70):
42 days (statutory maximum: 56 days)
Average period for fast-track review of COVID-19 files (n=14):
15 days
The MREC Utrecht also reviews VHP files.
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Medical device regulation as of 26 May 2021
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New adult subject information template
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Telephone consultation option resumed
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2019 Annual Report of the MREC Utrecht
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Coronavirus: Amended procedures
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Research with medical devices: MDR implementation postponed until 26 MAY 2021
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Overview news items
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Research with a medicinal product
More information on research with a medicinal product can be found on the CCMO intranet page.
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Research with a medical device
More information on research with medical devices can be found on the CCMO and IGJ intranet page.
- CCMO 'Research with a medical device from 26 May 2021'
- IGJ 'Klinische onderzoek met medisch hulpmiddel'
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Institutional policy
For questions and more information about your institution's policy on medical research involving human subjects, please see the pages below:
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Participating institutions: UMC Utrecht and Prinses Máxima Center for pediatric oncology