Clinical Trials

We can draw on our multidisciplinary, integrated knowledge for the following activities in clinical research:

  • Organisation and monitoring of trials according to GCP
  • Preparation of study documents according to GCP: protocols, CRFs, patient information, diaries, monitoring documents etc.
  • Preparation of SOPs: standard operating procedures for the monitoring and performance of trials
  • Quality assurance: several aspects during the performance and documentation of trials