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Clinical trial monitoring is part of the clinical trial quality management system. Our experienced Clinical Research Associates (CRAs) perform the monitoring tasks in accordance with the applicable regulations and CCDRD´s monitoring SOPs.

Monitoring services:

  • Site feasibility evaluation incl. feasibility questionnaire circulation
  • Site selection
  • Monitoring visits of clinical sites
  • Preparation of monitoring reports
  • Interaction with clinical sites and investigators
  • Tight communication and reporting to central project management at headquarters
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