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Page: Clinical investigation of medicinal products in the treatment of patients with acute respiratory distress syndrome - Scientific guideline-2025/2/28
2025-03-03查看详情 > -
国家药品不良反应监测年度报告(2024年)-2025/4/7
2025-04-08查看详情 > -
Document: Summary of changes to the ‘External guidance on the implementation of the European Medicines Agency policy on the publication of clinical data for medicinal products for human use’ - Version 1.5-2025/5/15
2025-05-16查看详情 > -
国家药监局关于抗感解毒片和舒筋活络止痛膏转换为非处方药的公告(2025年第60号)-2025/6/25
2025-06-26查看详情 > -
Document: Additional information - Applicant’s clarifications following Paediatric Committee (PDCO) discussions or re-discussions-2025/7/28
2025-07-29查看详情 > -
国家药监局关于同意安徽、江西、陕西省药监局开展优化药品补充申请审评审批程序改革试点的批复-2025/9/12
2025-09-12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 for production environment
2025-10-17查看详情 > -
Page: International Coalition of Medicines Regulatory Authorities (ICMRA)-2025/11/21
2025-11-24查看详情 > -
Sponsor Responsibilities - Safety Reporting Requirements and Safety Assessment for IND and Bioavailability/Bioequivalence Studies-2025/12/15
2025-12-16查看详情 > -
Document: HMA-EMA Network Data Steering Group: membership list-2026/1/28
2026-01-29查看详情 >