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1. Informasjonsskriv legemiddelutprøving (Clinical Trials Regulation (CTR))
2. Informasjonsskriv utprøving av medisinsk utstyr (MDR/IVDR)
3. Informasjonsskriv fremtidig forskning (CTR/MDR/IVDR)

English:

• The necessary information letter with a request for participation and a declaration of consent in accordance with a template shall be prepared as an appendix to the application.
• Click on the link below to download the template and save it on your own computer for further editing.
• After editing, the information letter must be uploaded as an attachment to the application form.

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1. Template – Informed Conset Form Clinical Trials Regulation (CTR)
2. Template – Broad Consent Future Reseach REK KULMU