Document: Questions and answers about the clinical study data proof-of-concept pilot for industry-2026/1/21

Page: EudraVigilance training and support-2026/2/24

Document: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure-2026/3/27

Document: European Medicines Agency's data protection notice for Modelling and Simulation Pilot - Use of clinical study data for scientific advice-2026/5/7

Guidance on good manufacturing practice and good distribution practice: Questions and answers-2022/10/26

Regulatory and procedural guideline: Guidance on the details of the classification of variations requiring assessment according to Article 62 of Regulation (EU) 2019/6 for veterinary medicinal products and on the documentation to be submitted pursuant to

关于公开征求《按古代经典名方目录管理的中药复方制剂药学申报资料撰写指导原则（征求意见稿）》意见的通知-2023/10/30

Document: Overview of comments received on the draft revision of EMA’s Policy on handling competing interests of scientific committee members and experts-2025/1/14

Document: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure: document with track changes-2025/2/18

Document: Three year work plan for the Good Manufacturing Practice / Good Distribution Practice Inspectors Working Group 2025-2027-2025/3/27