Enabling Future Health

Scandinavian CRO, SCRO, performs complete studies or parts of projects within the field of clinical studies. Both within Pharma and MedTech. We are a full-service contract research organisation (CRO) that helps manage trial aspects such as feasibility studies, study design, medical writing, site selection, submission to authorities and ethics committees, monitoring, site management and pharmacovigilance, as well as study documentation, data management, statistics, and good clinical practice (GCP) training to ensure clinical studies comply with national and international regulations.