
Comprehensive site management and monitoring services ensure trials are conducted smoothly, safely, and in compliance with regulations. Our comprehensive site Management & Monitoring process involves:
- Site identification and qualification
- Feasibility studies
- Site staff training
- Document management
- On-site monitoring
- Remote monitoring
- Risk-based monitoring
- Source data verification (SDV)
- Clinical trial material accountabilityRegulatory compliance
- Audit preparation and support
- Adverse event reporting
- Safety management
- Site close-out
- Final reporting
Through these site management processes, we’re able to ensure you deliver accurate, high-quality data avoiding unnecessary roadblocks or delays in the drug development process.
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