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Page: Data in regulation: Big data and other sources-2025/4/1
2025-04-02查看详情 > -
Document: Justification table templates-2025/5/13
2025-05-14查看详情 > -
Post-Warning Letter Meetings Under GDUFA-2025/6/20
2025-06-20查看详情 > -
Page: Portfolio and technology meetings-2025/7/24
2025-07-25查看详情 > -
Document: List of clinical evaluation consultation procedure (CECP) opinions issued for medical devices awaiting finalisation of conformity assessment-2025/9/10
2025-09-11查看详情 > -
Document: Timetable: Type II variation and worksharing application monthly assessment-2025/10/14
2025-10-15查看详情 > -
Page: Podcast: Inside EMA-2025/11/18
2025-11-19查看详情 > -
Document: Biomarkers in oncology indications approved in the EU: key facts-2025/12/12
2025-12-15查看详情 > -
Page: Scientific Advisory Group on Vaccines and Therapies for Infectious Diseases (SAG-V&ID)-2026/1/27
2026-01-28查看详情 > -
E2D(R1) Post-Approval Safety Data: Definitions and Standards for Management and Reporting of Individual Case Safety Reports-2026/3/3
2026-03-05查看详情 >
