Yes, Your Study is at Risk: Risk Mitigation Plans for Endpoints
Available on Demand
Trials that include ocular endpoints are uniquely exposed to operational risk, especially when off-site referrals, capacity constraints, and unclear workflows slow enrollment and drive avoidable deviations. In this actionable session, 20/20 Onsite’s Jessica McKenzie shares a field-tested framework to rapidly triage issues to maintain trial continuity with the sponsor and CROs.
You will see how to:
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Connect specific early-warning signals to clear triage actions, from tightening visit scheduling to adding on-site ophthalmic capacity.
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Align certified ophthalmic staff and validated equipment with existing sponsor and CRO workflows so data remains consistent during a rescue.
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Apply a reusable risk-mitigation checklist to your current protocol and leave with a path to request a zero-commitment, 24-hour assessment for your study.
Watch the Webinar Now!
Learn how to spot early warning signals in trials with ocular endpoints and apply a practical rescue playbook to protect timelines, data quality, and patient experience.
Key learning objectives:
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Identify real-world early warning signs that your ocular endpoints are at risk, including enrollment stalls, screen-fail spikes, off-site referral bottlenecks, and slow site activation.
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Translate those signals into immediate operational fixes by tightening scheduling, adding point-of-need ophthalmic capacity, and standardizing imaging and certification workflows.
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Use a simple decision framework to know when to adjust processes and capacity versus when a protocol or endpoint redesign is required, and how to partner for a rapid rescue.