首页 >
法规速递
-
国家药监局关于中药保护品种的公告(延长保护期第21号)(2025年第20号)-2025/2/25
2025-02-27查看详情 > -
Page: Data in regulation: Big data and other sources-2025/4/1
2025-04-02查看详情 > -
Document: Justification table templates-2025/5/13
2025-05-14查看详情 > -
Post-Warning Letter Meetings Under GDUFA-2025/6/20
2025-06-20查看详情 > -
Page: Portfolio and technology meetings-2025/7/24
2025-07-25查看详情 > -
Document: List of clinical evaluation consultation procedure (CECP) opinions issued for medical devices awaiting finalisation of conformity assessment-2025/9/10
2025-09-11查看详情 > -
Document: Timetable: Type II variation and worksharing application monthly assessment-2025/10/14
2025-10-15查看详情 > -
Page: Podcast: Inside EMA-2025/11/18
2025-11-19查看详情 > -
Document: Biomarkers in oncology indications approved in the EU: key facts-2025/12/12
2025-12-15查看详情 > -
Page: Scientific Advisory Group on Vaccines and Therapies for Infectious Diseases (SAG-V&ID)-2026/1/27
2026-01-28查看详情 >