Services

Monitoring

 

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