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Document: Quick guide: How to search, view and download a Clinical Trial and a Clinical Trial Application (sponsors) - CTIS Training Programme - Module 09-2025/2/18
2025-02-19查看详情 > -
Document: Product Management Service (PMS) roadmap-2025/3/26
2025-03-27查看详情 > -
Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2025/4/30
2025-05-06查看详情 > -
图解海报 |《医疗器械网络销售质量管理规范》系列解读（一）-2025/6/11
2025-06-12查看详情 > -
Page: Scientific and technical recommendations: Veterinary Medicines Regulation-2025/7/16
2025-07-17查看详情 > -
Document: List of centrally authorised products with safety-related changes to the product information-2025/8/29
2025-09-01查看详情 > -
Document: QRD Appendix V - Adverse-drug-reaction reporting details-2025/10/3
2025-10-08查看详情 > -
国家药监局关于中药保护品种的公告（延长保护期第25号）（2025年第112号）-2025/11/12
2025-11-13查看详情 > -
Page: European Sales and Use of Antimicrobials for Veterinary Medicine (ESUAvet) annual surveillance reports-2025/12/9
2025-12-10查看详情 > -
M4Q(R2) The Common Technical Document for the Registration of Pharmaceuticals for Human Use: Quality-2026/1/20
2026-01-21查看详情 >
