EFPIA：2025年欧洲试点项目概述测试电子产品信息（ePI）在药品中的应用报告（英文版）

In accordance with the current European legislation, a paper leaflet must be included in each pack of a medicinal product. This leaflet contains important information and guidance on the proper use of the respective medicinal product, approved by the competent regulatory authorities. The European pharmaceutical legislation is currently under review. The proposed revision includes the introduction of electronic patient information (ePI) and creates the possibility for the future transition fro