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Document: Annex to 16-19 June 2025 CHMP Agenda-2025/6/16
2025-06-17查看详情 > -
国家药监局关于修订复方甘草酸单铵S注射剂说明书的公告（2025年第72号）-2025/7/21
2025-07-22查看详情 > -
Page: Academia-2025/9/4
2025-09-05查看详情 > -
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 >
