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Document: Questions and answers to stakeholders on the implications of Regulation (EU) 2023/1182 for centrally authorised medicinal products for human use-2025/1/21
2025-01-22查看详情 > -
Document: European Medicines Agency procedural advice for users of the centralised procedure for similar biological medicinal products applications-2025/2/24
2025-02-25查看详情 > -
Document: Call for scientific data for the periodic review of the monograph on Valerianae radix and Lupuli flos-2025/4/1
2025-04-02查看详情 > -
Page: Careers-2025/5/8
2025-05-09查看详情 > -
国家药监局关于批准注册236个医疗器械产品的公告(2025年5月)(2025年第58号)-2025/6/19
2025-06-20查看详情 > -
Document: Origio - Procedural steps and scientific information after initial consultation (archive)-2025/7/25
2025-07-25查看详情 > -
Page: Pre-authorisation guidance-2025/9/8
2025-09-09查看详情 > -
Document: Applications for new human medicines under evaluation: October 2025-2025/10/10
2025-10-11查看详情 > -
Document: Medicinal products for human use: monthly figures - October 2025-2025/11/17
2025-11-18查看详情 > -
Document: Checklist for the submission of Day 215 product information annexes for a post-opinion linguistic review (Word file)-2025/12/12
2025-12-15查看详情 >
