Directive 8 Of 2024 Guidelines. Regulation (eu) 2017/745 on medical devices (mdr) and regulation (eu) 2017/746 (ivdr) on in vitro. Directive 2014/34/eu is a harmonisation directive (ce marking) and part of the new approach.
Volume 4 of the rules governing medicinal products in the european union contains guidance for the interpretation of the principles and guidelines of good manufacturing. The recast energy performance of buildings directive (epbd) (eu/2024/1275), adopted in may 2024, enhances the energy performance requirements for new buildings.