Imaging Risk Playbook: Endpoint Protection
How to avoid deviations, protect data, and keep trials on schedule.
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Close gaps, plan proactively, and build an imaging strategy that stands up to real-world execution and regulatory scrutiny.
100% On-Time • 80% Less Patient Travel • 70% Fewer Dropouts
Trusted across 40+ trials, 85,000 exams, and leading partners.





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LEARN HOW TO...
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Prevent protocol drift with harmonized imaging workflows across sites.
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Reduce screen-fail surprises with tighter BCVA/OCT standards.
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Keep timelines intact by eliminating off-site imaging travel drag.
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Ship audit-ready data with real-time QA and certified staff.
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"Imaging instruments are costly and require precision in their use. It's important to be proactive in creating an imaging strategy to not only have a plan in place but to work with a reliable, skilled team with a proven track record in producing high-quality images within study timelines. This strategic forethought will result in improved consistency and quality across all sites."
- Dr. Katherine Harkins, Director, Optometry, 20/20 Onsite
Trusted by leading sponsors, CROs, and sites
Point of Need
100%
Screening timelines met across all business operations.
Data Integrity
98%
Data accuracy submission rate.
Patient Retention
91%
Patient retention rate vs industry standard 70%.
Patient Centricity
95+
Patient NPS score.
Ocular Endpoint Protection Starts with the Right Strategy.
How 20/20 Onsite can help:
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Strategic Assessment - Comprehensive evaluation of your trial's imaging requirements, endpoint specifications, and regulatory pathway to identify optimal solutions.
Execution Excellence - Certified imaging staff, standardized protocols, and real-time quality assurance that deliver consistent, audit-ready data across all sites.
Proven Results - Track record of meeting 100% of screening timelines, decreasing patient dropout by 70%, and delivering data that withstands FDA scrutiny.