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《国家药监局关于无参比制剂品种仿制研究的公告》政策解读-2023/10/13
2023-10-13查看详情 > -
Document: Terms of Reference (ToR) for the International Medicines Regulators’ Working Group on 3Rs-2025/1/8
2025-01-09查看详情 > -
Document: QRD veterinary product-information template version 9.1-2025/2/14
2025-02-18查看详情 > -
Page: Pre-authorisation guidance-2025/3/25
2025-03-26查看详情 > -
Page: Measles-2025/4/28
2025-04-29查看详情 > -
Document: Minutes - PDCO minutes of the 22-25 April 2025 meeting-2025/6/5
2025-06-06查看详情 > -
Document: IRIS guide for applicants - How to create, submit and manage IRIS applications, for industry and individual applicants-2025/7/14
2025-07-15查看详情 > -
2025年8月21日中药品种保护受理公示-2025/8/21
2025-08-22查看详情 > -
Document: List of centrally authorised products with safety-related changes to the product information-2025/9/30
2025-10-08查看详情 > -
Page: Cancer medicines-2025/11/7
2025-11-10查看详情 >
