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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 > -
Document: Timetable: Companion diagnostic initial consultation-2025/10/3
2025-10-08查看详情 > -
Document: EVVet3 EVWeb Production - Release notes-2025/11/12
2025-11-13查看详情 > -
Document: List of substances and products subject to worksharing for signal management-2205/12/9
2025-12-10查看详情 > -
Document: Product Management Service (PMS) – Frequently Asked Questions (FAQs)-2026/1/21
2026-01-22查看详情 >