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Document: European Shortages Monitoring Platform (ESMP): Implementation guide for national competent authorities-2025/1/29
2025-02-05查看详情 > -
Document: Frequently asked questions (FAQs) : How to create and submit an annual safety report and respond to related requests for information - CTIS Training Programme - Module 18-2025/3/5
2025-03-06查看详情 > -
Document: ICH Guideline M13B on bioequivalence for immediate release solid oral dosage forms - additional strengths - Step 2b-2025/4/9
2025-04-11查看详情 > -
Document: Agenda - PDCO agenda of the 20-23 May 2025 meeting-2025/5/20
2025-05-21查看详情 > -
Cybersecurity in Medical Devices: Quality System Considerations and Content of Premarket Submissions-2025/6/27
2025-06-27查看详情 > -
Page: Rilpivirine product-specific bioequivalence guidance-2025/7/30
2025-07-31查看详情 > -
关于公开征求《研发期间安全性更新报告常见问答(征求意见稿)》意见的通知-2025/9/17
2025-09-18查看详情 > -
Document: Highlights – EMA/ EASD bilateral meeting-2025/10/22
2025-10-23查看详情 > -
Document: Minutes of the COMP meeting 7-8 October 2025-2025/11/25
2025-11-26查看详情 > -
Document: Recommended submission dates for veterinary medicinal products-2026/2/2
2026-02-03查看详情 >