Suitability of the facilities

Description of site suitability for each trial site. It is recommended to use the European Commission’s Site Suitability Template. The form must be issued by the head of department, head of clinic or an equivalent person at the institution who is not the study PI.

Important shortcuts

Update

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

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

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