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