08/24/2026
From rare disease and CNS to oncology, immunology, and ophthalmology, sponsors and CROs may need specialized ophthalmic assessments integrated into protocols, sites, workflows, and patient visits.
When those requirements are not planned or executed correctly, the warning signs can include enrollment stalls, screen-fail spikes, referral bottlenecks, slow site activation, and inconsistent data.
In our on-demand webinar, Yes, Your Study is at Risk: Risk Mitigation Plans for Endpoints, Jessica McKenzie shares a practical framework for identifying those risks early and determining the right operational response.
You’ll learn how to:
• Recognize early warning signs that ocular endpoints are at risk
• Add point-of-need ophthalmic capacity when needed
• Align certified staff and validated equipment with existing workflows
• Standardize imaging and certification processes
• Determine when an operational fix is enough, and when a protocol or endpoint redesign may be required
One accountable ophthalmic partner can make a complex requirement much easier to manage.
20/20 Onsite delivers specialized ophthalmic assessments wherever your trial requires them, helping sponsors and CROs protect timelines, data integrity, patient experience, and trial continuity.
Watch the webinar on demand:
https://hubs.ly/Q04tm8cs0