Clinical Site Monitoring
Clinical Site Monitoring
GRC professional CRAs work with sponsors and project teams during every phase of clinical study. Our Clinical Site Monitoring Services include:
- IEC/IRB Management:
- Regulatory Document Review:
- Data Verification:
- Contract and Budget Negotiation:
- On-Site Training:
- Site Qualification and Closeout:
- Interim Monitoring:
- Protocol Deviations:
- Drug Accountability:
- Close-out Visits:
These services ensure precision, compliance, and participant safety in clinical trials, leading to successful study completion.
