首页 >
法规速递
-
Draft Guidance: Acute Radiation Syndrome: Developing Drugs for Prevention and Treatment-2023/4/19
2023-04-24查看详情 > -
国家药监局关于中药保护品种的公告(延长保护期第12号)(2023年第127号)-2023/10/16
2023-11-06查看详情 > -
Document: Records of data processing activity for of the EMA's historical archives and opening to the public-2025/1/9
2025-01-10查看详情 > -
Document: EU Implementation Guide (IG) on veterinary medicines product data in the Union Product Database - Chapter 2: Format for the electronic submission of veterinary medicinal product information-2025/2/17
2025-02-18查看详情 > -
Document: European Medicines Agency procedural advice on recommendations on unforeseen variations according to Article 5 of Commission Regulation (EC) No 1234/2008-2025/3/25
2025-03-26查看详情 > -
国家药监局关于发布《化妆品中甲基泼尼松的测定》化妆品补充检验方法的公告(2025年第47号)-2025/4/30
2025-05-06查看详情 > -
国家药监局关于发布二代基因测序相关体外诊断试剂分类界定指导原则的通告(2025年第22号)-2025/6/10
2025-06-11查看详情 > -
Document: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure: document with track changes-2025/7/15
2025-07-16查看详情 > -
Page: Assessment templates and guidance-2025/8/26
2025-08-27查看详情 > -
Document: Products Management Services (PMS) - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe - Chapter 1: Registration requirements-2025/10/2
2025-10-08查看详情 >