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Regulatory and procedural guideline: IRIS guide to registration and RPIs-2023/4/20
2023-04-24查看详情 > -
国家药监局关于加强药品上市许可持有人委托生产监督管理工作的公告（2023年第132号）-2023/10/23
2023-11-06查看详情 > -
国家药监局关于批准注册259个医疗器械产品的公告（2024年12月） （2025年第4号）-2025/1/10
2025-01-10查看详情 > -
Page: Template for a European Union herbal monograph-2025/2/17
2025-02-18查看详情 > -
国家药品抽检年报（2024）-2025/3/27
2025-03-27查看详情 > -
Document: Business process description for expert management-2025/4/30
2025-05-06查看详情 > -
Document: Day 80 assessment report - Non-clinical template with guidance - Rev 06.25 Revamp-2025/6/10
2025-06-11查看详情 > -
Page: Grouping of variations: questions and answers-2025/7/15
2025-07-16查看详情 > -
CVM GFI #236 Clarification of FDA and EPA Jurisdiction Over Mosquito-Related Products-2025/8/27
2025-08-28查看详情 > -
Page: Other fees and charges for medicinal products for human use, veterinary medicinal products and consultations on medical devices-2025/10/2
2025-10-08查看详情 >
