IND vs IMPD: Building One Data Package That Satisfies Both FDA & EU Regulators
Executive snapshot Filing separate first-in-human (FIH) dossiers for the United States and Europe can drag an early-stage program six-plus months behind plan. A harmonised approach—one Common Technical Document (CTD) “master” that slots into both the FDA Investigational New Drug (IND) sequence and the EU Clinical Trials Regulation (CTR) portal (CTIS)—cuts review-cycle queries by ~35 %, […]
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