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Business · 15/05/2015

FDA Releases Draft Guidance for Industry on Investigational New Drug Applications

The Food and Drug Administration (FDA) has made available a draft guidance document to help sponsor-investigators prepare and submit complete Investigational New Drug Applications (INDs) to the FDA's Center for Drug Evaluation and Research (CDER) and Center for Biologics Evaluation and Research (CBER).

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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