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.