In my role as a GCP-coordinator I provide guidance to doctors in the public sector according to requirement for trial related documents and approval from the authorities. I perform monitoring of clinical trials before, during and after data collection taking into account EU and national legislation and the international guideline ICH GCP. In addition, I am part of organizing the GCP unit's 3-day PhD course, perform audits and report SUSARs for researchers in the Central Jutland region.