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Document: European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure-2025/12/15
2025-12-16查看详情 > -
国家药监局综合司关于2026年医疗器械行业标准制修订计划项目公示-2026/1/28
2026-01-28查看详情 > -
Page: Orphan designation: Overview-2026/3/6
2026-03-09查看详情 > -
国家药监局关于修订注射用过氧化碳酰胺说明书的公告（2026年第35号）-2026/4/7
2026-04-08查看详情 > -
E19 A Selective Approach to Safety Data Collection in Specific Late-Stage Pre-Approval or Post-Approval Clinical Trials (Final)-2022/12/5
2022-12-06查看详情 > -
Scientific guideline: Concept paper on the development of a guideline on the quality aspects of mRNA vaccines-2023/6/23
2023-06-25查看详情 > -
国家药监局关于修订复方首乌地黄丸说明书的公告（2023年第160号）-2023/12/27
2024-01-03查看详情 > -
国家药监局关于简化港澳已上市传统口服中成药内地上市注册审批的公告（2025年第7号） -2025/1/21
2025-01-23查看详情 > -
Page: Website outages and upgrades-2025/2/26
2025-02-27查看详情 > -
Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2025/4/2
2025-04-03查看详情 >
