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Document: European Medicines Agency’s data protection notice for the management of traineeships at EMA-2026/5/5
2026-05-06查看详情 > -
Document: Timetable: Type II variation and worksharing application alternative monthly assessment-2026/6/16
2026-06-17查看详情 > -
ICH guideline S1B(R1) on testing for carcinogenicity of pharmaceuticals-2022/10/10
2022-11-15查看详情 > -
国家药监局关于修订环磷腺苷注射剂说明书的公告（2023年第49号）-2023/4/24
2023-04-25查看详情 > -
国家药监局综合司 海关总署办公厅关于增设黑龙江省绥芬河、同江药材进口边境口岸有关事项的通知-2023/10/27
2023-11-06查看详情 > -
Premarket Approval Application and Humanitarian Device Exemption Modular Review-2025/1/13
2025-01-14查看详情 > -
Page: International Coalition of Medicines Regulatory Authorities (ICMRA)-2025/2/17
2025-02-18查看详情 > -
Page: List of medicines under additional monitoring-2025/3/26
2025-03-27查看详情 > -
Document: List of medicinal products under additional monitoring-2025/4/30
2025-05-06查看详情 > -
Document: Network Portfolio Roadmap-2025/6/10
2025-06-11查看详情 >
