Clinical Monitoring
As a kind of “quality safety net”, our experienced experts monitor the implementation of your study and thus support you in achieving a high-quality output.
Depending on the individual requirements of your project for the monitoring strategy, we offer you different approaches.
What we offer
On-Site monitoring
- Visits by our monitors / CRAs on site at the trial centre
- Focus on declarations of consent/data protection, source data verification, source data review
Centralised monitoring
- Risk-based approach – focus on critical data and processes
- Systematic and timely data analysis of eCRF data and data from other electronic systems
- Review by monitors / CRAs / data managers / statisticians
- Safety and coding review
Remote monitoring
- Telephone monitoring / video conferencing
- Plausibility and completeness checks in an eCRF or other electronic systems