Document: Medicinal products for human use: monthly figures - March 2025-2025/4/16

Document: Overview of comments received on 'Reflection paper on the application of Article 40(5) of Regulation (EU) 2019/6 for certain categories of variations' (EMA/CVMP/55240/2025)-2025/6/2

关于公开征求《化学仿制药参比制剂目录（第九十五批）》（征求意见稿）意见的通知-2025/7/4

国家药监局关于养心定悸胶囊转换为非处方药的公告（2025年第74号）-2025/8/7

Document: Timetable: Post-authorisation measure (PAM) assessed by CAT-2025/9/24

Document: European Medicine Agency's data protection notice for the Interactive Regulatory Information System (IRIS)-2025/11/3

Document: Questions and answers on implementation of the medical devices and in vitro diagnostic medical devices Regulations ((EU) 2017/745 and (EU) 2017/746) - tracked changes-2025/12/2

国家药监局关于修订异维A酸软胶囊说明书的公告（2026年第2号）-2026/1/6

Document: Validation checklist for Type II quality variations-2026/2/10

Document: List of withdrawn medicinal products in accordance with Art. 123(4) of the Directive (1 January - 31 December 2025)-2026/3/19