EU GMP Annex 13 Investigational Medicinal Products 2010

Source of this document: Eudralex document ENTR/F/2/AM/an D(2010) 3374 of 3 February 2010 with full title “The Rules Governing Medicinal Products in the European Union, Volume 4, EU Guidelines to Good Manufacturing Practice, Medicinal Products for Human and Veterinary Use, Annex 13: Investigational Medicinal Products”, published by European Commission‘s Enterprise and Industry Directorate-General, © European Union, 2010.

Permission for reproduction (2010-COP-197 A 152915) granted to PharmDev Innovations GmbH by the Publications Office of the European Union. No liability is assumed for correct transscript of the official text.