首页 >
法规速递
-
Document: HMA-EMA joint Network Data Steering Group meeting - 16 September 2025-2025/10/7
2025-10-08查看详情 > -
Page: Classification of a product as intended for a limited market and eligibility for authorisation under Article 23 of Regulation (EU) 2019/6 (Applications for limited markets)-2025/11/14
2025-11-17查看详情 > -
Page: How to submit information on authorised and investigational medicines-2025/12/10
2025-12-11查看详情 > -
Page: Requirements for combined vaccines and associations of immunological veterinary medicinal products (IVMPs) - Scientific guideline-2026/1/23
2026-01-26查看详情 > -
Document: Draft concept paper on the development of a reflection paper on the non-clinical development and evaluation of microbiome-based medicinal products-2026/3/2
2026-03-03查看详情 > -
Document: Timetable: Initial (full) marketing authorisation application assessment-2026/3/27
2026-03-30查看详情 > -
Document: Agenda of the CAT meeting 11-13 May 2026-2026/5/11
2026-05-12查看详情 > -
Document: Fee regulation working arrangements-2026/6/24
2026-06-25查看详情 > -
他达拉非片生物等效性研究技术指导原则-2022/11/25
2022-11-25查看详情 > -
国家药监局综合司再次征求《药品标准管理办法（征求意见稿）》意见-2023/5/5
2023-05-06查看详情 >
