Participation of industry experts in the elaboration of monographs and chapters of the European Pharmacopoeia

    loading  Checking for direct PDF access through Ovid


The European Pharmacopoeia represents an important element in the European regulatory system for medicines. It is elaborated in a co-operation of experts from authorities, academia and industry, assisted by scientific staff from the European Directorate for the Quality of Medicines & HealthCare (EDQM). This article describes the principles of its elaboration with particular focus on the involvement of industry experts.

Related Topics

    loading  Loading Related Articles