首页 >
法规速递
-
Document: Draft guideline on good pharmacovigilance practices (GVP): Module XVI Addendum I – Educational materials-2025/6/2
2025-06-03查看详情 > -
Document: Meeting summary of the Medicine Shortages SPOC Working Party meeting on 13 May 2025-2025/7/7
2025-07-08查看详情 > -
Document: Superseded - Composition of the Emergency Task Force (ETF) for preparedness-2025/8/7
2025-08-10查看详情 > -
Expedited Programs for Regenerative Medicine Therapies for Serious Conditions-2025/9/24
2025-09-25查看详情 > -
Document: Agenda of the CVMP meeting 4-6 November 2025-2025/11/3
2025-11-04查看详情 > -
Document: HMA-EMA joint Network Data Steering Group meeting - 6 October 2025-2025/12/3
2025-12-04查看详情 > -
Page: Healthcare Professionals' Working Party-2026/1/6
2026-01-07查看详情 > -
Document: Agenda of the CVMP meeting 10-12 February 2026-2026/2/10
2026-02-11查看详情 > -
Document: IRIS guide for applicants - How to create, submit and manage IRIS applications, for industry and individual applicants-2026/3/19
2026-03-20查看详情 > -
国家药监局关于发布药品附条件批准上市申请审评审批工作程序的公告(2026年第41号)-2026/4/24
2026-04-27查看详情 >