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Home / REK KULMU / Introduction to REK KULMU / REK KULMU Comittees
  • 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 of clinical investigations (MDR)
    • Combination studies
    • Modifications to clinical investigations
  • Performance studies (IVDR)
    • Application for ethical assessment of performance studies under the IVDR
    • Combination trials
    • 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

REK KULMU Comittees

REK KULMU COMMITTEE A:
Members 1 July 2025 – 30 June 2029:

  • Committee chair Bjørn Øglænd. Representation: Medicine, Paediatrics
  • Deputy chairperson Anne Elise Eggen. Representation: Medicine
  • Deputy chairperson Elisabeth Gjefsen. Representation: Medicine
  • Benedicte Paus. Representation: Medicine: Genetics
  • Tone Veiteberg. Representation: Medical technical device and in vitro medical device
  • Markus Jerkø. Representation: Law
  • Espen Dyrnes Stabell. Representation: Ethics
  • Kjetil Korslund. Representation: Lay representative
  • Gunnhild Berglen. Representation: Patient and user organisation

 

REK KULMU COMMITTEE B:
Members 1 July 2025 – 30 June 2029:

  • Committee chair Gry Dahle. Representation: Medicine
  • Deputy chairperson Hege Thoresen. Representation: Pharmacy
  • Deputy chairperson Heidi Glosli. Representation: Medicine, Paediatrics
  • Anders Waage. Representation: Medicine
  • Nora Leerberg. Representation: Law
  • Fred-Johan Pettersen. Representation: Medical technical device and in vitro medical device
  • Attila Tanyi. Representation: Ethics
  • Øystein Kydland. Representation: Lay representative
  • Cicel Aarrestad. Representation: Patient and user organisation

 

COMMON SUBSTITUTES FOR THE REK KULMU COMMITTEES:

  • Torstein Baade Rø. Representation: Medicine: Paediatrics
  • Beate Hennie Garcia. Representation: Pharmacy
  • Wenche Grønnvold. Representation: Medical technical device and in vitro medical device
  • Øystein Flø Baste. Representation: Law
  • Kristine Bærøe. Representation: Ethics
  • Yvonne Hording. Representation: Lay representative
  • Sissel S. Ohm. Representation: Lay representative

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)
Illustrasjon av leger

Current messages

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  • 14. Aug 2026

Update

Approved REK KULMU applications are not displayed in NVA (the Norwegian Research Information Repository)

Applications to REK KULMU submitted after 1 July 2026 will not be visible in NVA. This is because NVA...

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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...

Read more

REK

General inquiries should be directed to the REK in your geographical region.

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 / REK KULMU
    • About REK
    • Introduction to REK KULMU
    • Project registry
    • Postjournal
  • Application form
    • Prosjektsøknad
    • Generell biobank
    • Dispensasjon fra taushetsplikt annen forskning
    • CTIS
  • Templates REK KULMU
  • EN
  • NO
  • About REK / REK KULMU
    • About REK
    • Introduction to REK KULMU
    • Project registry
    • Postjournal
  • Application form
    • Prosjektsøknad
    • Generell biobank
    • Dispensasjon fra taushetsplikt annen forskning
    • CTIS
  • Templates REK KULMU
  • EN
  • NO
Project register

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 of clinical investigations (MDR)
    • Combination studies
    • Modifications to clinical investigations
  • Performance studies (IVDR)
    • Application for ethical assessment of performance studies under the IVDR
    • Combination trials
    • 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