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Page: Contacting EMA: post-authorisation-2026/6/15
2026-06-16查看详情 > -
In Vitro Release Test Studies for Topical Drug Products Submitted in ANDAs (Draft)-2022/10/21
2022-11-15查看详情 > -
国家药监局药审中心关于发布《儿童用药沟通交流中Ⅰ类会议申请及管理工作细则（试行）》的通告-2023/4/18
2023-04-24查看详情 > -
Scientific guideline: Guideline on the calculation of dose factor to be submitted to the Union Product Database (UPD)-2023/10/13
2023-10-16查看详情 > -
Document: European Medicines Agency’s data protection notice for the processing of personal data contained in the Agency’s historical records selected for permanent preservation and opening to the public-2025/1/9
2025-01-10查看详情 > -
Document: Contact details of national competent authorities for requests of translation exemptions falling under Art. 63.3 of Directive 2001/83/EC and cases of shortages-2025/2/17
2025-02-18查看详情 > -
Page: Notifying a change of marketing status-2025/3/25
2025-03-26查看详情 > -
Document: CTIS newsflash - 29 April 2025-2025/4/29
2025-04-30查看详情 > -
关于公开征求《先进治疗药品的范围、归类和释义（征求意见稿）》意见的通知-2025/6/10
2025-06-11查看详情 > -
Document: Checklist for the submission of product information annexes and Annex A (if applicable) for minor procedures without linguistic review - human-2025/7/15
2025-07-16查看详情 >
