首页 >
法规速递
-
Document: Agenda of the HMPC meeting 7-9 July 2025-2025/7/4
2025-07-07查看详情 > -
2025年8月8日中药品种保护受理公示-2025/8/8
2025-08-10查看详情 > -
Document: Timetable: Post-authorisation measure (PAM) assessed by PRAC-2025/9/24
2025-09-25查看详情 > -
Document: Records of data processing activity for Early Notification System (ENS)-2025/11/3
2025-11-04查看详情 > -
Document: Agenda of the CVMP meeting 2-4 December 2025-2025/12/2
2025-12-03查看详情 > -
《国家药监局关于加强药品受托生产监督管理工作的公告》政策解读-2026/1/6
2026-01-07查看详情 > -
Page: Ledipasvir/sofosbuvir product-specific bioequivalence guidance-2026/2/10
2026-02-11查看详情 > -
Document: EU Implementation Guide (IG) on veterinary medicines product data in the Union Product Database - Chapter 5: Technical specifications-2026/3/19
2026-03-20查看详情 > -
Page: Procurement and grants-2026/4/22
2026-04-23查看详情 > -
国家药监局综合司关于印发2023年药品检验能力验证计划的通知-2023/03/09
2023-03-09查看详情 >
