首页 >
法规速递
-
Document: Frequently asked questions on the European Shortages Monitoring Platform (ESMP)-2025/12/16
2025-12-17查看详情 > -
Document: Concept paper for the development of a reflection paper on the use of Bayesian methods in clinical development-2026/1/30
2026-02-02查看详情 > -
Document: SMS guidance for external users-2026/3/10
2026-03-11查看详情 > -
Document: Veterinary medicine safety day: Why read veterinary medicines package leaflet-2026/4/8
2026-04-09查看详情 > -
Document: Questions and answers on periodic safety update report single-assessment (PSUSA): Guidance document for assessors-2026/5/22
2026-05-25查看详情 > -
Document: Working arrangement for the collaboration and exchange of information on therapeutic products and medicinal products between DG SANTE/EMA and the New Zealand Ministry of Health-2026/7/8
2026-07-09查看详情 > -
Document: Presentation - The safe hearts plan (Y. Azzopardi)-2026/8/13
2026-08-14查看详情 > -
国家药监局药审中心关于发布《药物临床试验盲法指导原则（试行）》的通告（2022年第49号）-2022/12/30
2022-12-30查看详情 > -
国家药监局综合司关于《药品网络销售禁止清单（第一版）》有关问题的复函-2023/7/10
2023-07-10查看详情 > -
国家药监局综合司公开征求《关于优化已在境内上市的境外生产药品转移至境内生产的 药品上市注册申请相关事宜的公告》意见-2024/1/24
2024-02-05查看详情 >
