Design CRFs That Won’t Derail Your Eye Care Trial
Get the 1-page checklist and avoid rejected data, extra work, and delays.
"I was a neophyte to clinical research and have enjoyed working with you because you are very patient and have offered very helpful guidance in the mechanics of how these studies are designed, submitted, presented, published, etc. "
What you get:
✅ Avoid missing ophthalmology-specific data points (like OD/OS, refraction, IOP)
✅ Ensure your CRFs align with your study endpoints
✅ Make your data clean, codable, and publication-ready
✅ Simplify your IRB and monitoring documentation
What is it all about?
Designing case report forms (CRFs) for eye care studies is harder than it looks.
Most templates aren't built with ophthalmology in mind — so critical fields like laterality, refraction, or surgical details get missed. Even well-meaning forms can cause delays in IRB approvals, monitoring issues, or unusable data at analysis.
This checklist gives you a clear, expert-backed framework for building CRFs that meet publication standards, regulatory expectations, and real-world clinical workflows — without wasting time on formatting or second-guessing.
Whether you're preparing a single-center pilot or a multicenter trial, this 1-page reference helps you get it right the first time.