• Identification and qualification of high-performing research sites • Feasibility assessments and regulatory approvals • Study startup support, including IRB/EC submissions
Regulatory Compliance & Documentation
• Ensuring compliance with ICH-GCP, FDA, EMA, and other global regulations • Management of essential trial documentation • Audit readiness and inspection support
Data Collection & Reporting
• Continuous site monitoring for protocol adherence and data accuracy • Patient recruitment and retention strategies • Investigator and site staff training
Site Management & Monitoring
• Real-time data monitoring for accuracy and completeness • Efficient query resolution and documentation review • Electronic Data Capture (EDC) system support
Services provide for you
Site Partner SMO LLP offers a full suite of services to support clinical trials from start to finish.
