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Document: Veterinary medicines safety day: Adverse event reporting in the EU - presentation-2025/4/8
2025-04-09查看详情 > -
Document: Medicinal products for human use: monthly figures - April 2025-2025/5/19
2025-05-20查看详情 > -
Document: PRIME: 5 years' experience-2025/6/26
2025-06-27查看详情 > -
国家药监局药审中心关于发布《发酵或半合成化学仿制药抗生素有关物质限度制定指导原则》的通告（2025年第28号）-2025/7/30
2025-07-31查看详情 > -
国家药监局综合司关于印发医疗器械注册自检核查指南的通知-2025/9/16
2025-09-17查看详情 > -
2025年10月21日中药品种保护受理公示-2025/10/21
2025-10-22查看详情 > -
Document: PRAC recommendations on signals adopted at the 27-30 October 2025 PRAC meeting-2025/11/24
2025-11-25查看详情 > -
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 >
