Do not miss this opportunity to expand your knowledge and familiarise yourself with the the Procedure of Certification of Suitability to the monographs of the European Pharmacopoeia (CEP).
Workshop sessions will cover :
· How to build a good CEP dossier – including the Top 10 Deficiencies and the control of elemental impurities
· GMP inspections of API manufacturers
· How to successfully prepare electronic submissions for CEP applications
All relevant information on this conference and the full programme can be found HERE.
Registrations can be submitted HERE.