De-Risking the Neurology IND: Lessons from Early FDA Engagement
Neurology INDs face unique complexities: subjective endpoints, variable outcomes, and substantial investments. Our white paper reveals how early FDA engagement—6-9 months before submission—transforms regulatory risk into predictable success. Drawing from 200+ neurology programs over the past five years, learn proven strategies for productive pre-IND meetings, avoiding common pitfalls, and building collaborative agency relationships that accelerate your path to first-in-human trials.
Download our expert guide to early FDA engagement and position your neurology program for IND success.
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