首页 >
法规速递
-
Document: Minutes of the CVMP meeting 10-12 June 2025-2025/10/16
2025-10-17查看详情 > -
《药品生产企业出口药品检查和出口证明管理规定》政策解读-2025/11/21
2025-11-24查看详情 > -
Investigator Responsibilities – Safety Reporting for Investigational Drugs and Devices-2025/12/15
2025-12-16查看详情 > -
Document: Minutes of the HMPC meeting 17-19 November 2025-2026/1/28
2026-01-29查看详情 > -
Page: Organisation Management Service (OMS)-2026/3/9
2026-03-10查看详情 > -
Document: CHMP PROM minutes for the meeting on 14 July 2025-2026/4/7
2026-04-08查看详情 > -
中药新药用于胃食管反流病的临床疗效评价技术指导原则（试行）-2022/12/21
2022-12-22查看详情 > -
国家药品监督管理局批准西罗莫司凝胶上市-2023/6/30
2023-06-30查看详情 > -
ICH Q2(R2) Validation of analytical procedures - Scientific guideline-2023/12/22
2024-01-03查看详情 > -
Page: Veterinary medicinal products for zootechnical purposes - Scientific guideline-2025/1/24
2025-02-05查看详情 >
