Site capabilities
Operational infrastructure for clinical trial execution
ACRC is equipped to support sponsors and CROs across Phase I–IV studies — from Feasibility to Start-up, Contract & Budget, Regulatory, Recruitment, Study Conduct and Subject Retention, and study close-out.
Clinical & laboratory
- On-site phlebotomy and centrifugation
- ECG / EKG and vitals monitoring
- Temperature-controlled IP storage (ambient, refrigerated, frozen)
- Specimen processing, shipping, and chain-of-custody
- On-site exam rooms and infusion-ready space
Regulatory & start-up
- Central and local IRB submissions
- 1572, FDF, financial disclosures, and CV management
- Protocol training and delegation log management
- Rapid site activation and CTA negotiation support
Patient access & recruitment
- Active patient database across therapeutic areas
- Community outreach and physician referral network
- Digital and traditional recruitment campaigns
- Bilingual study staff
Quality & compliance
- ICH-GCP trained investigators and coordinators
- Source-document driven with audit-ready files
- EDC-fluent coordinators with low query rates
- Standardized SOPs and ongoing staff training