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Home / New layout in the REC portal
  • 20. Jun 2025

New layout in the REC portal

The REK portal has undergone a necessary upgrade that involves some changes in appearance and layout.

Here is an overview of what’s new and how to navigate the portal:

For prosjektleder/ansvarshavende:

1. Your applications

  • – You can find all your applications under the tab “Min portefølje” and “Mine saker”.
  • – Here, you will also see related communication, and any tasks (documents that need to be addressed) associated with the applications.

2. Inquiries from REK that require a response (tasks)

  • – Inquiries from REK that require your response are displayed under the tab “My Portfolio” and “My Cases”.
    • The inquiry is linked to the relevant application and is shown in the overview of your cases.
  • – To read and respond to an inquiry, click on the link marked in blue on the right side of the overview.

3. Other communication related to applications

  • – When you select one of the applications from your overview, you will find all communication related to the application under the tab “Dokumenter”.

4. Submitting “Endringsmelding” (Project changes) or “Sluttmelding” (Final report)

  • – To submit project changes or final report:
    • – Select the relevant application.
    • Click on the “Options” button
    • – Choose either “Endring og/eller henvendelse” (Change and/or inquiry) or “Sluttmelding” (Final report) from the menu.

For co-users: (Medbruker):

  • – Applications shared with you can be found under the tab “Min portefølje” and “Delt med meg”.

Current messages

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  • 20. Jun 2025

Update

New layout in the REC portal

The REK portal has undergone a necessary upgrade that involves some changes in appearance and layout. Here is an...

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  • 14. Feb 2025

CTRIVDRMDR

Updated templates for informed consent forms

There are updated templates for informed consent forms for studies that are regulated by CTR, MDR or IVDR at...

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  • 24. Nov 2024

How to activate 2-step verification when logging in to REK-portalen

It is now possible for users of the REK portal to activate 2-step verification when logging in to REK-portalen....

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Important shortcuts

  • DMPs website
  • Templates REK KULMU
  • Regulatory guide for clinical trials according to the MDR (only available in Norwegian)
  • DMPs website
  • Templates REK KULMU
  • Regulatory guide for clinical trials according to the MDR (only available in Norwegian)
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REK KULMU

For questions regarding the ethical assessment of clinical trials under CTR, MDR, and IVDR, please contact via email: rek-kulmu@medisin.uio.no

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    • About REK
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REK

  • About REC

REK KULMU

  • REK KULMU Comittees
  • Meetings
  • REK KULMU
  • Clinical Trials Regulation (CTR)
    • EU application portal CTIS
    • General requirements and recommendations for a CTR application
      • Modification application CTIS
      • Part I application
      • Part II application (national application)
        • Recruitment
        • Information to study participants and consent form
        • Suitability of the investigator
        • Suitability of the facilities
        • Proof of insurance cover or indemnification
        • Financing and other arrangements
        • Compliance with national requirements on Data Protection
        • Compliance with use of biological samples
          • Use of biological material for future research
  • Clinical investigations of medical devices (MDR)
    • Application to REK for MDR studies
    • Clinical trials of medical device that are subject to application or notification to NoMA
    • Combination trials
    • Storage period of personal data
    • Modification applications to NoMA
  • Clinical investigations of in vitro diagnostic medical devices (IVDR)
    • Application to REK for IVDR studies
    • Performance studies that are subject to application or notification to NoMA
    • Combination trials
    • Storage period of personal data
    • Modification application performance studies
  • Information forms CTR/MDR/IVDR
    • Inclusion of minors in reserach
    • Informed consent forms for broad consent
  • Templates REK KULMU
  • Answers to frequently asked questions