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Page: Lurasidone product-specific bioequivalence guidance-2025/6/30
2025-07-01查看详情 > -
Page: Business hours and holidays-2025/7/31
2025-08-01查看详情 > -
Document: Procedural advice on appointment and responsibilities of the CVMP rapporteur and co-rapporteur in accordance with Article 140(6) of Regulation (EU) 2019/6, and peer reviewer-2025/9/19
2025-09-22查看详情 > -
Document: Agenda of the PRAC meeting 27 - 30 October 2025-2025/10/27
2025-10-28查看详情 > -
Page: Submitting results of paediatric studies-2025/11/26
2025-11-27查看详情 > -
国家药监局关于发布互联网药品医疗器械信息服务备案管理规定的公告（2025年第123号）-2025/12/22
2025-12-23查看详情 > -
Document: European Medicines Agency’s data protection notice for EudraVigilance Human (EV)-2026/2/5
2026-02-06查看详情 > -
Page: Union Product Database-2026/3/13
2026-03-16查看详情 > -
Document: Article 57 product data-2026/4/14
2026-04-15查看详情 > -
Regulatory and procedural guideline: Guideline on the application of Article 34 of Regulation (EU) 2019/6-2023/01/27
2023-01-27查看详情 >
