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国家药监局关于发布《医疗器械生产许可与备案管理基本数据集》等2个信息化标准的公告 （2025年第75号）-2025/8/1
2025-08-04查看详情 > -
Page: The procedure to be followed when a batch of a vaccine finished product is suspected to be contaminated with bovine viral diarrhoea virus - Scientific guideline-2025/9/19
2025-09-22查看详情 > -
关于公开征求《主方案设计的药物临床试验指导原则（征求意见稿）》意见的通知-2025/10/28
2025-10-29查看详情 > -
Document: Questions and answers on implementation of the medical devices and in vitro diagnostic medical devices Regulations ((EU) 2017/745 and (EU) 2017/746) - tracked changes-2025/11/26
2025-11-27查看详情 > -
Page: Funding-2205/12/22
2025-12-23查看详情 > -
Document: Procedural advice for vaccine platform technology master file (vPTMF) certification-2026/2/5
2026-02-06查看详情 > -
Page: Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG)-2026/3/13
2026-03-16查看详情 > -
Document: Radiopharmaceuticals EU-IN Horizon Scanning Report-2026/4/15
2026-04-16查看详情 > -
Q8, Q9, and Q10 Questions and Answers (R5) -2026/5/29
2026-05-31查看详情 > -
Scientific guideline: Reflection paper on resistance in ectoparasites-2023/01/27
2023-01-27查看详情 >
