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Menu
  • Home
  • Submission
    • WMO applicable
    • Non WMO research
    • Approval Board of Directors UMCG
    • Biobank
  • Topics
    • Adverse Events (SAEs, SUSARs, SADEs, etc.)
    • Recruiting and informing the potential subject.
    • Research with minors and incapacitated subjects
    • The role of the treating physician and investigator
  • Documents
  • Information & Contact
    • METc – bureau
    • Composition METc UMCG
    • METc UMCG meetings
    • METc UMCG Fee
    • More practical information
  • FAQ
  • News
    • Meeting dates 2021
    • Brexit and possible consequences for clinical research
    • Clinical Trial Regulation expected to apply from December 2021
    • New template Subject Information Sheet is mandatory from November 2020.
    • CCMO will be the competent authority for clinical investigations with medical devices
    • Modified procedure for submitting local feasibility declaration
    • What is the impact of the GDPR on the informed consent letter?
    • Conditions for (re)starting clinical research in healthcare institutions and CRUs aligned
  • English
    • Dutch
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Submission

Here you will find information on the submission procedure for your research proposal whether it

  • is Medical Research Involving Human Subjects (in Dutch: WMO, Wet medisch wetenschappelijk onderzoek met mensen)
  • is non-WMO
  • has already been reviewed
  • is a Biobank.

 

For every submission we request you send the documentation as separate PDF files on a CD Rom or USB drive. When it is a medical research with human subjects the files should be named and listed according to the Standard Research File, as described by the CCMO (please visit their website for this document).

Furthermore, all the scientific research conducted in the University Medical Center Groningen must be listed in the UMCG Research Registry before submission to the METc UMCG.

Please contact the Servicedesk Clinical Research Office for more information on the UMCG Research Registry via Clinical-research-office@umcg.nl.

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