The Procedure of Certification of Suitability to the Monographs of the European Pharmacopoeia (CEP) is an important tool for regulators and industry in preparing, assessing and managing marketing authorisations for medicinal products. The aim of this conference is to trace recent evolutions and changes of the Certification Procedure in a fast moving regulatory environment.

Expert speakers from industry and authorities from all over the world will present their experience. Particular importance will also be given to new developments and the place of the procedure in a globalised world.