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
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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.
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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.
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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.
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Mobile clinics reduce participation barriers, enable more inclusive trials, deliver representative data, speed timelines, and advance equity in research.
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Remote ophthalmic assessments such as BCVA, OCT, and IOP expand trial access and efficiency, preserving data quality while reducing site burden and boosting patient engagement.
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Clinical research sites often face ophthalmic endpoint challenges, causing delays, deviations, dropouts, and burnout. Check out the four-step framework to overcome these issues efficiently.
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GLP1 and neurology trials depend on detecting subtle retinal or neuro-ophthalmic changes early. By planning an imaging strategy upfront, sponsors can de-risk studies and protect critical endpoints.
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How can you turn capacity limits into enrollment momentum and ensure timelines stay on track while also expanding access to diverse patient populations?
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While GLP-1 receptor agonists offer significant health benefits, proactive eye care and vigilance are essential to mitigate the risk of irreversible ocular conditions.
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Explore the necessity of incorporating imaging methodologies early in the trial design to improve data quality and overall trial efficiency.
CONTACT INFORMATION
20/20 Onsite
29 Garden Street
Everett, MA 02149
UNITED STATES
Phone: 617-812-9453
Contact: Jessica McKenzie, Vice President, Life Sciences