The organization may consider whether it is appropriate to conduct accompanying research during the implementation of the AI system or other forms of research to contribute to experience sharing. If so, it is necessary to establish contact with relevant research groups, define the objectives and scope of the research, and secure funding for the work. This aspect should be considered before the tender documents for the procurement are announced. Clinical research must be approved by the Regional Committees for Medical and Health Research Ethics (REK), and clinical investigations of medical devices must be approved by the Norwegian Medical Products Agency (DMP).
Example: Northern Norway Regional Health Authority has financed an accompanying research project at the Norwegian National Centre for E-health Research (NSE) on the benefits and values of introducing commercial AI solutions in the field of radiology in Northern Norway Regional Health Authority.