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Page: Certification of medicinal products-2025/1/6
2025-01-07查看详情 > -
Page: Product-specific bioequivalence guidance-2025/2/10
2025-02-11查看详情 > -
Page: CVMP recommendations on limited market classification and eligibility for authorisation under Article 23-2025/3/18
2025-03-19查看详情 > -
Document: Template for late submission of ICSRs to EV-2025/4/22
2025-04-23查看详情 > -
Document: Meeting summary - Medicine shortages (SPOC) working party 10-11 April 2025-2025/6/2
2025-06-03查看详情 > -
国家药监局综合司再次公开征求《药品附条件批准上市申请审评审批工作程序（试行）（修订稿征求意见稿）》及政策解读意见-2025/7/8
2025-07-09查看详情 > -
Document: Paediatric investigation plan (PIP) - Key elements form-2025/8/8
2025-08-10查看详情 > -
Page: Medicine Shortages Single Point of Contact (SPOC) Working Party-2025/9/25
2025-09-26查看详情 > -
Page: Medicine shortages and availability issues-2025/11/4
2025-11-05查看详情 > -
Document: HMPC: overview of assessment work - priority list-2025/12/3
2025-12-04查看详情 >
