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Document: Questions & answers - Practical arrangements on the companion diagnostics consultation procedure to the European Medicines Agency by notified bodies-2025/4/11
2025-04-13查看详情 > -
2025年05月26日中药品种保护受理公示-2025/5/26
2025-05-27查看详情 > -
Page: ICH E20 adaptive designs for clinical trials - Scientific guideline-2025/6/30
2025-07-01查看详情 > -
Medical Device User Fee Small Business Qualification and Determination -2025/7/31
2025-08-01查看详情 > -
Page: Duration of immunity achieved by veterinary vaccines - Scientific guideline-2025/9/19
2025-09-22查看详情 > -
关于将芦沃美替尼片纳入“儿童抗肿瘤药物研发鼓励试点计划（“星光计划”）”试点项目的通知-2025/10/28
2025-10-29查看详情 > -
Page: Transfer of marketing authorisation: questions and answers-2025/11/26
2025-11-27查看详情 > -
Document: List of centrally authorised products with safety-related changes to the product information-2025/12/22
2025-12-23查看详情 > -
Document: Procedural advice for veterinary vaccine antigen master file (VAMF) certification-2026/2/5
2026-02-06查看详情 > -
Page: Data protection and privacy at EMA-2026/3/13
2026-03-16查看详情 >
