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Clinical trial monitoring

aCROnordic is active in clinical trial monitoring across Denmark, Sweden, Norway, and Finland. Furthermore, we work through an extensive global partner network. We have wide experience in organising, coordinating, and executing national and multinational phase I-IV clinical studies in accordance with the ICH GCP Guidelines and FDA/EMEA regulations.


Our clinical trial monitoring services cover:

  • Organisation of investigator and monitor meetings 
  • Trial master file setup and maintenance
  • Site visits (pre-trial, initiation, interim monitoring, close-out) 
  • In-house site management 
  • Patient progress tracking 
  • Preparation of and participation in audit and inspection