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Page: Product-specific bioequivalence guidance-2024/1/15
2024-02-05查看详情 > -
Document: List of industry subject matter experts and list of planned calls for industry subject matter experts-2025/1/29
2025-02-05查看详情 > -
Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2025/3/5
2025-03-06查看详情 > -
Document: Minutes of the PRAC meeting 13-16 May 2024-2025/4/9
2025-04-11查看详情 > -
Document: Scientific recommendations on classification of advanced therapy medicinal products-2025/5/21
2025-05-22查看详情 > -
Document: Questions and answers on the outcome of assessment on use of Revolade in treatment of severe aplastic anaemia in children-2025/6/27
2025-06-30查看详情 > -
Page: Ticagrelor product-specific bioequivalence guidance-2025/7/30
2025-07-31查看详情 > -
图解海报 | 《中药生产监督管理专门规定》发布（二）-2025/9/17
2025-09-18查看详情 > -
国家药监局关于发布仿制药参比制剂目录（第九十七批）的通告（2025年第37号）-2025/10/23
2025-10-24查看详情 > -
Document: Product Management Service (PMS) – Frequently Asked Questions (FAQs)-2025/11/25
2025-11-26查看详情 >
