20/20 Onsite

ABOUT US

20/20 Onsite is a healthcare services company providing clinical trial solutions that transform the delivery of vision care by radically improving patient access through state-of-the-art Mobile Vision Clinics. 20/20 Onsite's integrated point-of-need service delivery platform has taken high-value eye assessment services directly to patients at work, at school, in neighborhoods, and at clinical research sites. During the pandemic, 20/20 Onsite began bringing ophthalmic assessments to patients in clinical trials or post-marketing safety surveillance programs nationwide, increasing access to clinical research. 20/20 Onsite enables and accelerates fundamental trends toward the consumerization of care and the decentralization of clinical trials.

20/20 Onsite has served over 85,000 patients, including 22 clinical trials, met 100% of screening timelines across operations, and consistently reports patient NPS scores of over 94.

FEATURED ARTICLES

Ocular Hypertension In Clinical Trials: Protecting IOP Endpoints From Execution Risk

Fluctuations in eye pressure measurements can jeopardize trial results. Learn how standardized execution and equipment calibration protect data integrity and regulatory credibility.
Ophthalmology Clinical Trials: Why Sponsors Are Prioritizing This Therapeutic Area

Explore how demographic shifts and retinal innovation are transforming ophthalmology trials, and why operational precision is the key to protecting data integrity in this high-growth sector.
Patient Centric Clinical Trials: Why Transportation Is A Timeline Risk

Address transportation barriers to reduce protocol deviations and data gaps. Strategies that lower travel burden protect study timelines and improve visit adherence for better trial outcomes.
How To Reduce Patient Dropout Rates In Clinical Trials

Sponsors are addressing patient dropout rates by shifting from reactive troubleshooting to proactive protocol designs that minimize participant burden.
BCVA, OCT, And IOP Testing In Clinical Trials

Are minor inconsistencies in room setup and technician technique quietly compromising your study data? Learn how closing small operational gaps can prevent major downstream risks.
Site Initiation Visits For Clinical Trials: Ocular Endpoint Planning For Sponsors And CROs

Learn how expert site initiation visit (SIV) planning masters complex endpoints like OCT and BCVA, eliminates data variability, and prevents the costly need for trial rescue.
The Clinical Trial Rescue Triage Playbook

Quickly assess clinical trial risks by evaluating site impact, patient safety, and budget tradeoffs. Turn high-pressure rescue scenarios into clear, actionable paths for your research team.
At-Home Clinical Trials: When At-Home Ophthalmic Exams Make Sense

At-home ophthalmic exams in clinical trials improve patient accessibility, reduce site burden, and maintain data integrity, enabling decentralized research without sacrificing quality or compliance.
Why Clinical Trial Demographics Don't Match Real-World Populations

Representative trial demographics reduce bias, strengthen safety insights, and ensure therapies work for all. Learn why diversity is essential for accurate data and better health outcomes.
How Mobile Clinics Advance Diversity In Clinical Research

Mobile clinics reduce participation barriers, enable more inclusive trials, deliver representative data, speed timelines, and advance equity in research.