He European Directive 2001 / 83 on medicinal products lays down constraints on drugs via Common Technical Documents consisting of 5 modules. The key to this regulation as it sets the framework for quality module 4 (pre-clinical part) is dedicated to technology and module 5 to clinical assessments.
He European Directive 2001 / 83 on medicinal products lays down constraints on drugs via Common Technical Documents consisting of 5 modules. The key to this regulation as it sets the framework for quality module 4 (pre-clinical part) is dedicated to technology and module 5 to clinical assessments.
He European Directive 2001 / 83 on medicinal products lays down constraints on drugs via Common Technical Documents consisting of 5 modules. The key to this regulation as it sets the framework for quality module 4 (pre-clinical part) is dedicated to technology and module 5 to clinical assessments.