首页 >
法规速递
-
国家药监局综合司公开征求《药品生产质量管理规范》血液制品附录（修订稿征求意见稿）意见-2023/12/26
2024-01-03查看详情 > -
中药保护品种公告(第22号)(2025年第8号) -2025/1/21
2025-01-23查看详情 > -
Document: Agenda - PDCO agenda of the 25-28 February 2025 meeting-2025/2/26
2025-02-27查看详情 > -
Document: Joint HTAb-regulatory perspectives on understanding evidence challenges, managing uncertainties and exploring potential solutions-2025/4/2
2025-04-03查看详情 > -
Document: European Shortages Monitoring Platform (ESMP) essentials: Industry and network reporting requirements-2025/5/13
2025-05-14查看详情 > -
Document: Management Board meeting dates 2026-2027-2025/6/20
2025-06-23查看详情 > -
Document: European Union Member State Public Holidays Recorded in CTIS (year: 2026)-2025/7/25
2025-07-27查看详情 > -
关于公开征求《抑郁障碍治疗药物临床试验技术指导原则（征求意见稿）》意见的通知-2025/9/11
2025-09-12查看详情 > -
Document: Guide on access to unpublished documents-2025/10/14
2025-10-15查看详情 > -
图解海报 | 《国家药监局关于深化化妆品监管改革促进产业高质量发展的意见》系列解读（三）-2025/11/19
2025-11-20查看详情 >
