For Pharma & Clinical Research
The functional vision data your trial is missing between visits.
Capture continuous patient-generated functional vision data between site visits for stronger endpoints, earlier signal detection, and real-world evidence beyond the clinic.
The Challenge
Site visits capture moments.Trials need trajectories.
EyeCTester extends your visibility window from quarterly snapshots into a continuous functional record without adding site visits or patient travel.
Outcomes For Trials
What continuous endpoints enable
Continuous Real-World Evidence
Longitudinal functional data supports regulatory submissions, post-market evidence requirements, and commercial differentiation.
Earlier Signal Detection
See the shape of response curves rather than only scheduled snapshots.
Reduced Site Burden
Remote daily testing lowers coordinator burden and can improve enrollment and retention.
Regulatory-Ready Data Output
Structured, audit-trailed exports accelerate submission preparation.
Trial Infrastructure
Trial-ready infrastructure
FDA 510(k) Cleared SaMD
Validated under the FDA regulatory framework for visual function assessment.
Standardized 4-test battery
Visual Acuity, Contrast Sensitivity, Color, and Amsler & Central Visual Field in a protocol-ready workflow.
HIPAA-compliant infrastructure
AWS-hosted, role-based access controls, and breach procedures support clinical operations.
Protocol-aligned configuration
Visit schedule, test frequency, alert thresholds, and assessment windows can be configured per protocol.
Multi-site ready
Centralized sponsor dashboard with site-level visibility and multilingual patient support.
Therapeutic Areas
Validated across therapeutic areas
Explore EyeCTester for your clinical program.
Partnering with pharma and research teams in retina, glaucoma, and neuro-ophthalmology.