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Document: Factsheet - Industry reporting via the European Shortages Monitoring Platform (ESMP) in normal circumstances-2025/12/16
2025-12-17查看详情 > -
Document: List of industry subject matter experts and list of planned calls for industry subject matter experts-2026/1/30
2026-02-02查看详情 > -
Page: Class III implantable devices and Class IIb medical devices intended to administer or remove medicinal products: expert panel opinions-2026/3/9
2026-03-10查看详情 > -
国家药监局药审中心关于发布《药物临床试验申请临床评价技术指导原则》的通告（2026年第27号）-2026/4/8
2026-04-09查看详情 > -
国家药监局关于潞党参口服液转为非处方药的公告（2022年第104号）-2022/12/28
2022-12-29查看详情 > -
Regulatory and procedural guideline: Guidance on Parallel EMA/HTA body (HTAb) Scientific Advice for the Interim Period-2023/7/3
2023-07-05查看详情 > -
国家药监局药审中心关于发布《药物免疫毒性非临床研究技术指导原则》的通告（2024年第5号）-2024/1/18
2024-01-19查看详情 > -
Document: Minutes of the CAT meeting 4-6 December 2024-2025/1/28
2025-02-05查看详情 > -
Document: Infectious Diseases Working Party (IDWP) consolidated 3-year rolling work plan 2025-2027-2025/2/28
2025-03-03查看详情 > -
Document: List of signals discussed at PRAC since September 2012-2025/4/7
2025-04-08查看详情 >
