We ensure that every aspect of your study is aligned with its ocular endpoints, resulting in compliant trial designs that meet critical timelines and schedules. With a proven track record of refining protocols for numerous multi-center studies, we consistently improve clinical trial outcomes.

• Expertly aligning ocular assessments with study endpoints to ensure robust, compliant trial designs and maintain budgets, timelines, and schedules.
• Tailoring patient recruitment and protocol strategies to enhance efficiency and safeguard trial success.

Our prescreening process harnesses advanced analytics and targeted outreach to identify the candidates for your clinical study. By thoroughly evaluating patient profiles early on, we significantly reduce screening times and ensure that only the best-fit participants move forward.

• Utilizes data-driven insights to target and identify ideal candidates precisely.
• Streamlines initial outreach and evaluation, reducing screening time and enhancing candidate suitability.

Our patient enrollment strategy is centered on creating a smooth and engaging enrollment process that minimizes barriers to entry. We combine point-of-need assessments with personalized support to efficiently enroll patients while strictly adhering to regulatory standards.

• Implements a user-friendly, patient-centric exam assessment schedule to improve patient engagement.
• Ensures swift, compliant onboarding that accelerates the start of your clinical trial.

We integrate directly into your clinical trial workflow, ensuring that each ophthalmic assessment perfectly aligns with study requirements and does not disrupt your current site workflow. This integration reduces disruptions and maintains the integrity of critical data throughout the trial.

• Synchronizes point-of-need vision clinics with established clinical workflows for seamless execution.
• Optimizes exam workflows to ensure continuous, high-quality data collection and minimal process disruption.

Our retention strategy recognizes that ongoing patient engagement is vital for trial success and emphasizes continuous communication and point-of-need support. We proactively keep participants informed, engaged, and motivated throughout the study.

• Employs proactive communication, scheduling, and follow-up strategies to sustain engagement.
• Uses educational tools and support to foster a positive trial experience.

Ensure that trial patients continue to receive the follow-up assessments required by your study, wherever they are. Our point-of-need assessments help analyze long-term outcomes to keep patient safety at the forefront.

• Conducts comprehensive point-of-need assessments to evaluate real-world effectiveness and long-term outcomes.
• Keep patient safety and compliance at the forefront with our point-of-need, flexible post-market solutions.