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.
- 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