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国家药监局综合司公开征求《麻醉药品和精神药品实验研究管理规定（征求意见稿）》意见-2023/11/6
2023-11-07查看详情 > -
Page: Financial advantages of SME status-2025/1/15
2025-01-16查看详情 > -
Document: Clinical Trial Information System (CTIS) - Sponsor handbook-2025/2/19
2025-02-20查看详情 > -
国家药监局综合司公开征求《关于优化全生命周期监管 支持高端医疗器械创新发展的举措（征求意见稿）》意见-2025/3/31
2025-04-01查看详情 > -
Document: PRAC recommendations on signals adopted at the 7-10 April 2025 meeting-2025/5/5
2025-05-06查看详情 > -
Document: Release notes - production release version 1.7.2523 - 16 June 2025 - Veterinary Medicinal Products Regulation: Union Product Database-2025/6/16
2025-06-17查看详情 > -
关于公开征求《化学仿制药参比制剂目录（第九十六批）》（征求意见稿）意见的通知-2025/7/18
2025-07-21查看详情 > -
Document: EU Implementation Guide (IG) on veterinary medicines product data in the Union Product Database - Chapter 4: Process and format for the submission of legacy data on veterinary medicinal products (obsolete)-2025/9/2
2025-09-03查看详情 > -
Page: CAT: Working parties and other groups-2025/10/6
2025-10-08查看详情 > -
Document: Concept paper on a paediatric update of the guideline on clinical investigation of medicinal products for the management of Crohn’s disease-2025/11/13
2025-11-14查看详情 >
