EU Guide to Good Manufacturing Practice for Medicinal Products for Human and Veterinary Use

This brochure contains the second official edition of the EU Guide to Good Manufacturing Practice (GMP), the corresponding Commission Directives for GMP for medicinal products and investigational medicinal products for human use and for veterinary medicinal products as well as a glossary.Having been restructured in 2005 and further revised later on, the current EU GMP Guide comprises three parts: Part I Basic Requirements for Medicinal Products, Part II Basic Requirements for Active Substances used as Starting Materials, and Part III GMP Relate ...