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Guidance on good manufacturing practice and good distribution practice: Questions and answers-2022/10/26
2022-11-15查看详情 > -
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
2023-04-26查看详情 > -
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
2023-11-07查看详情 > -
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
2025-01-15查看详情 > -
Document: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure: document with track changes-2025/2/18
2025-02-19查看详情 > -
Document: Three year work plan for the Good Manufacturing Practice / Good Distribution Practice Inspectors Working Group 2025-2027-2025/3/27
2025-03-28查看详情 > -
Document: Small and medium-sized enterprise (SME) office annual report 2024-2025/5/2
2025-05-06查看详情 > -
Document: User guide of the HMA-EMA Catalogues of real-world data sources and studies-2025/6/12
2025-06-13查看详情 > -
Document: Timetable: Annual reassessment-2025/7/17
2025-07-18查看详情 > -
Document: Organisation chart: Administration and Corporate Management-2025/9/1
2025-09-02查看详情 >