Regulatory and procedural guideline: Guidance on handling scientific committee/other (scientific) expert group member’s declared intention to become an employee in a pharmaceutical company, a medical device company or in the biotechnology sector (updated)

Document: Decision of the Management Board amending budget No. 04, amending appropriations in budget 2024-2025/1/7

2024年度医疗器械注册工作报告-2025/2/13

Document: Agenda of the CHMP meeting 24-27 March 2025-2025/3/24

Document: Report - Industry stakeholders and EU network experts surveys on early engagement fostering innovation-2025/4/23

Page: CHMP opinions on consultation procedures-2025/6/4

Page: Fees payable to the European Medicines Agency: Fees, charges and remuneration for assessment procedures and services relating to veterinary medicinal products-2025/7/10

Document: Records of data processing activity for EMA Authentication Services and Microsoft Entra ID-2025/8/19

Document: List of signals discussed at PRAC since September 2012-2025/9/29

国家药监局关于注销膝关节系统等10个医疗器械注册证书的公告（2025年第108号）-2025/11/6