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Premarket Approval Application and Humanitarian Device Exemption Modular Review-2025/1/13
2025-01-14查看详情 > -
Page: International Coalition of Medicines Regulatory Authorities (ICMRA)-2025/2/17
2025-02-18查看详情 > -
Page: List of medicines under additional monitoring-2025/3/26
2025-03-27查看详情 > -
Document: List of medicinal products under additional monitoring-2025/4/30
2025-05-06查看详情 > -
Document: Network Portfolio Roadmap-2025/6/10
2025-06-11查看详情 > -
Document: List of EU Medicines Regulatory Agency Organisation with single and multiple LOC IDs for Product Management Services (PMS) data enrichment - Chapter 2 Annex III-2025/7/15
2025-07-16查看详情 > -
关于公开征求《化学仿制药参比制剂目录（第九十七批）》（征求意见稿）意见的通知-2025/8/28
2025-08-29查看详情 > -
Page: Fees payable to the European Medicines Agency-2025/10/2
2025-10-08查看详情 > -
Document: Nanotechnology-based medicinal products for human use EU-IN Horizon Scanning Report-2025/11/11
2025-11-12查看详情 > -
Document: Alzheimer’s disease EU-IN Horizon Scanning Report-2025/12/9
2025-12-10查看详情 >
