Marianne Esbjerg

Title

GCP Coordinator

Primary affiliation

Marianne Esbjerg

Areas of expertise

  • GCP
  • Clinical drug trial
  • Monitoring
  • Investigation of medical device

Contact information

Telephone number
Email address

Job responsibilities

I advise public researchers conducting clinical drug trials or medical device investigations on the design of trial documents and submissions to authorities. I monitor trials before, during, and after data collection, and my work is based on the international guidelines for Good Clinical Practice (ICH-GCP) and the guideline for Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155).