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Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2026/2/4
2026-02-05查看详情 > -
Page: Veterinary antibiotics: Dosage review and adjustment (ADRA) project-2026/3/12
2026-03-13查看详情 > -
国家药监局关于复方氯化钠滴眼液处方药转换为非处方药的公告（2026年第36号）-2026/4/10
2026-04-10查看详情 > -
Regulatory and procedural guideline: Validation checklist for Type II (non) clinical variations (updated)-2023/01/05
2023-01-05查看详情 > -
国家药监局药审中心关于发布《罕见疾病药物开发中疾病自然史研究指导原则》的通告（2023年第43号）-2023/7/27
2023-07-28查看详情 > -
国家药监局关于修订祖卡木制剂、金刚藤制剂和斑秃丸说明书的公告（2024年第11号）-2024/2/6
2024-03-11查看详情 > -
Document: Member states contact points for translations review-2025/1/31
2025-02-05查看详情 > -
Document: European Shortages Monitoring Platform (ESMP) Application Programming Interface (API) specifications-2025/3/10
2025-03-11查看详情 > -
Document: Minutes - PDCO minutes of the 25-28 February 2025 meeting-2025/4/10
2025-04-11查看详情 > -
Document: Overview of comments received on ICH E6(R3) guideline for good clinical practice – Annex 2 - Step 2b-2025/5/23
2025-05-26查看详情 >
