For institutions

SOP Roller og ansvar i kliniske legemiddelutprøvinger og utprøving av medisinsk utstyr (Roles and responsibilities in clinical trials of medicinal products and studies of medical devices) should be adapted to the institution and be included in the institution’s quality system.

Furthermore, all NorCRIN’s procedures for clinical trials of medicinal products must be embedded in the institution’s quality system. One way this can be done is by referring to NorCRIN’s procedures in the institution’s research procedure.