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法规速递
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Page: List of medicines under additional monitoring-2025/9/26
2025-09-28查看详情 > -
Page: Good pharmacovigilance practices (GVP)-2025/11/4
2025-11-05查看详情 > -
Document: Veterinary Scientific Advice procedure – timelines 2026 - information for applicants-2025/12/4
2025-12-05查看详情 > -
Page: Medical devices-2026/1/12
2026-01-13查看详情 > -
Page: Paediatric investigation plans-2026/212
2026-02-13查看详情 > -
国家药监局关于同意福建、河南省药监局开展优化药品补充申请审评审批程序改革试点的批复-2026/3/24
2026-03-25查看详情 > -
Page: Expert panel support for breakthrough medical devices: pilot programme-2026/4/28
2026-04-29查看详情 > -
Document: Appendix 1: Acceptable intakes established for N-nitrosamines-2026/6/9
2026-06-10查看详情 > -
关于公开征求《非无菌化学药品及原辅料微生物限度研究技术指导原则（征求意见稿）》意见的通知-2022/10/10
2022-11-14查看详情 > -
关于公开征求《已上市境外生产药品转移至境内生产的药品上市注册申请申报资料要求（化学药品）（征求意见稿）》意见的通知-2023/03/23
2023-03-23查看详情 >
