With our team of experienced clinical research associats (CRA), we work closely with trial sites and data management to cover all areas of monitoring throughout Germany.
- Recruitment of trial sites / screening sites for eligibility
- Development of the monitoring plan
- Conducting initiation visits to ensure a smooth start to the trial
- Project specific training for all participants
- On-site and remote monitoring
- Centralized monitoring
- Ongoing site support between monitoring visits
- Unblinded Monitoring
- Conducting close-out visits to ensure proper study completion
- Co-Monitoring
- Supporting sites during audits and inspections
