Clinical Trials Office Denmark provides services for both researchers and the industry and creates contacts across sectors and regions

Our main target is to attract more clinical trials to Denmark. We do this by providing services which facilitate access to clinical trials in Denmark. Companies and CRO’s can therefore make use of Clinical Trials Office Denmark to:

  • Get contact information on potential sites/investigators
  • Assess the feasibility of conducting a clinical trial in Denmark
  • Get access to data from the Danish National Registry of Patients, which allows immediate determination of the number of patients with the relevant diagnosis seen in the hospitals and outpatient clinics during the previous years. It is not possible to identify individual patients and patient recruitment is carried out by local doctors without use of registries and according to the regulations of The Danish Research Ethics Committee
  • Access to national negotiation of contracts and preparation of Clinical Trial Agreement templates
  • Clarify general questions concerning clinical research in Denmark - specific application questions must still be processed by relevant Danish authorities (i.e. Danish Health and Medicines Authority, a Regional Committee on Health Research Ethics and the Danish Data Protection Agency)