Our Services
End-to-end clinical trial support, from protocol design through imaging analysis, delivered with the speed, structure, and responsiveness modern studies demand.
Operational depth and scientific precision at every stage of your ophthalmic trial.
Our service portfolio is designed to help sponsors simplify complexity, maintain quality, and keep studies moving from first protocol decisions to final image analysis.
Protocol Development
Design imaging protocols aligned with your scientific objectives, regulatory standards, and participant safety. Engage at feasibility stage - before the protocol is locked.
Site Selection & Management
Identify, qualify, and support clinical sites throughout the trial. Ensures imaging infrastructure meets study requirements from Day 1.
Device Certification
Fast certification of imaging devices across all sites. Consistency and data integrity guaranteed from first scan.
Photographer Certification
Certify site photographers to study-specific acquisition protocols. Reproducible, high-quality images from every site, every visit.
Lane & BCVA Certification
Remote Lane and BCVA Certification via the Clarity App - no in-person visit required. Mobile-first. Eliminates the most common cause of study startup delays.
Eligibility Assessment
Real-time eligibility reads against inclusion/exclusion criteria. <1 hour TAT available. Supports on-site randomization.
Image Analysis & Endpoints
Expert grading with AI-assisted pre-screening. Dual read + adjudication workflow. Proprietary algorithms (IGMP, StarGauge) integrated where needed. Audit-ready output.
Why Sponsors Choose OIRRC
- <1 hour eligibility TAT
- <1 week study startup
- 24/7 global operations
- 60+ trials completed
- AI-powered pre-screening
- Human-verified reads
- SOC 2, HIPAA, GDPR, ISO aligned
- FDA/EMA-ready data packages