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Document: Silapo : EPAR - All Authorised presentations-2026/8/4
2026-08-05查看详情 > -
Regulatory and procedural guideline: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure: document with track changes-2022/11/4
2022-11-30查看详情 > -
关于公开征求ICH《E6(R3):药物临床试验质量管理规范(GCP)》指导原则及附件1草案的通知-2023/5/29
2023-05-30查看详情 > -
国家药监局药审中心关于发布《药品说明书(简化版)及药品说明书(大字版)编写指南》和《电子药品说明书(完整版)格式要求》的通告(2023年第56号)-2023/11/24
2023-11-28查看详情 > -
Document: New fee regulation Annex IV: General questions and answers-2025/1/20
2025-01-21查看详情 > -
Document: Infectious Diseases Working Party (IDWP) consolidated 3-year rolling work plan 2025-2027-2025/2/21
2025-02-24查看详情 > -
Document: Call for scientific data for the periodic review of the monograph on Hamamelidis cortex-2025/4/1
2025-04-02查看详情 > -
Document: Process for the electronic submission of medicinal product information - Chapter 3-2025/5/8
2025-05-09查看详情 > -
Document: Antimicrobial Sales and Use (ASU) Platform: Release notes-2025/6/18
2025-06-19查看详情 > -
药你知道 | 《国家药监局关于发布优化全生命周期监管支持高端医疗器械创新发展有关举措的公告》系列解读(二) -2025/7/23
2025-07-24查看详情 >