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图解海报 | 《医疗器械生产质量管理规范》系列解读（三）-2025/11/12
2025-11-13查看详情 > -
Document: Consolidated 3-year rolling work plan for the Methodology Working Party 2026-2028-2025/12/9
2025-12-10查看详情 > -
Minimal Residual Disease and Complete Response in Multiple Myeloma: Use as Endpoints to Support Accelerated Approval-2026/1/21
2026-01-21查看详情 > -
Document: EudraVigilance - EVWEB user manual-2026/2/24
2026-02-27查看详情 > -
Document: European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure: document with tracked changes-2026/3/27
2026-03-30查看详情 > -
《医药代表管理办法》政策解读-2026/5/7
2026-05-08查看详情 > -
Page: How to recognise scams and phishing using EMA credentials-2026/6/18
2026-06-21查看详情 > -
《国家药监局关于化妆品注册备案有关事项的公告》政策解读-2026/7/29
2026-07-30查看详情 > -
ICH M11 guideline, clinical study protocol template and technical specifications-2022/10/26
2022-11-15查看详情 > -
国家药监局关于修订乙酰谷酰胺注射剂说明书的公告（2023年第57号）-2023/4/25
2023-04-26查看详情 >
