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Page: Plant testing strategy in the risk assessment for veterinary medicinal products - Scientific guideline-2026/3/20
2026-03-23查看详情 > -
Document: Minutes of the CVMP meeting 10-12 February 2026-2026/4/24
2026-04-27查看详情 > -
药监政策速览（第51期）：新版《药品召回管理办法》11月1日起施行-2022/11/1
2022-11-14查看详情 > -
Electronic Systems, Electronic Records, and Electronic Signatures in Clinical Investigations: Questions and Answers(Draft)-2023/03/15)
2023-03-15查看详情 > -
关于公开征求《仿制药质量和疗效一致性评价受理审查指南（征求意见稿）》意见的通知-2023/9/25
2023-09-26查看详情 > -
Document: IRIS guide for applicants - How to create and submit scientific applications, for industry and individual applicants-2025/1/6
2025-01-07查看详情 > -
Document: Agenda of the CVMP meeting 11-13 February 2025-2025/2/11
2025-02-12查看详情 > -
国家药监局关于废止《医用中心吸引系统通用技术条件》等2项医疗器械行业标准的公告（2025年第31号）-2025/3/19
2025-03-20查看详情 > -
Document: Business process description for orphan status management-2025/4/22
2025-04-23查看详情 > -
Document: Agenda - Workshop on the use of Bayesian statistics in clinical development-2025/6/3
2025-06-04查看详情 >
