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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Why Clinical Pharmacology and Regulatory Strategy Are Critical for Emerging Biotechs

Emerging biotech companies—and small to midsize pharma firms—face extraordinary constraints. Timelines are compressed, funding is finite, and regulatory expectations continue to evolve. These pressures make it essential to have a strategic development plan that integrates scientific rigor, operational efficiency, and regulatory foresight from the earliest stages. Biotech innovation is advancing at remarkable speed—but development timelines,

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