Routine On-site monitoring
Routine on-site monitoring is a pivotal component of clinical trial management, ensuring data integrity, patient safety, and protocol compliance. Clinical monitors conduct regular visits to investigational sites to:
- Review source documents and trial documentation.
- Verify data accuracy through source data verification (SDV).
- Ensure strict adherence to the trial protocol.
- Assess patient safety and adverse event reporting.
- Promptly address any identified issues through collaboration with site staff and investigators.
This hands-on approach guarantees data quality, regulatory compliance, and the highest standards of patient care in clinical trials.
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