首页 >
法规速递
-
Page: Clinical investigation of medicinal products for the treatment of psoriatic arthritis - Scientific guideline-2025/9/30
2025-10-08查看详情 > -
Document: Clinical Trial Information System (CTIS) - Sponsor handbook-2025/11/7
2025-11-10查看详情 > -
Document: Agenda - HMA/EMA Annual Data Forum 2025-2025/12/5
2025-12-08查看详情 > -
Document: 3-year rolling work plan for the Quality Innovation Group (QIG) 2026-2028-2026/1/15
2026-01-16查看详情 > -
Document: Minutes of the CHMP meeting 19-22 May 2025-2026/2/16
2026-02-26查看详情 > -
Document: Mobile scanning and other technologies in the labelling and/or package leaflet of centrally authorised medicinal products-2026/3/25
2026-03-26查看详情 > -
Page: VICH GL18(R2) impurities: residual solvents in new veterinary medicinal products, active substances and excipients - Scientific guideline-2026/4/29
2026-04-30查看详情 > -
User Fees and Refunds for Premarket Notification Submissions (510(k)s) (Final)-2022/10/5
2022-11-15查看详情 > -
成人用药数据外推至儿科人群的定量方法学指导原则（试行）-2023/4/12
2023-04-13查看详情 > -
国家药监局关于化学原料药再注册管理等有关事项的公告（2023年第129号）-2023/10/13
2023-10-13查看详情 >
