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The Investigational Medicinal Product Dossier - rpd-ch.com

Description: The Investigational Medicinal Product Dossier The Investigational Medicinal Product Dossier Regulatory Requirements: Based on Directive 2001/20/EC (“Clinical Trials Directive”) request for conducting a clinical trial (Art. 9.2) details on formats to be determined by EU Commission and Member States (Art 9 8)and Member States (Art. 9.8)

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