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Document: Members of the Coordinating group of European network of paediatric research at the European Medicines Agency (Enpr-EMA)-2025/2/10
2025-02-11查看详情 > -
Document: Advice to medical device manufacturers - 2025 Timetable-2025/2/10
2025-02-11查看详情 > -
Document: Request for advice on the clinical development strategy and / or clinical investigations according to Article 61(2) of Regulation (EU) 2017/745 on from the medical device expert panels-2025/2/10
2025-02-11查看详情 > -
Document: Guide to manufacturers on the procedure for requesting advice from expert panels on clinical investigations and / or clinical development strategies for high-risk medical devices-2025/2/10
2025-02-11查看详情 > -
Page: Linguistic review - Human-2025/2/10
2025-02-11查看详情 > -
Page: Industry Standing Group-2025/2/7
2025-02-10查看详情 > -
Page: PRIME: priority medicines-2025/2/7
2025-02-10查看详情 > -
Document: Recommendations on eligibility to PRIME scheme - Adopted at the CHMP meeting of 27-30 January 2025-2025/2/7
2025-02-10查看详情 > -
Page: Procurement-2025/2/7
2025-02-10查看详情 > -
Document: List of medicines currently in PRIME scheme-2025/2/7
2025-02-10查看详情 >
