首页 >
法规速递
-
Document: Veterinary pre-submission meeting request form - in accordance with Regulation (EU) No 2019/6-2026/3/3
2026-03-04查看详情 > -
Page: Pharmaceutical industry-2026/3/31
2026-04-01查看详情 > -
Document: HMPC: overview of assessment work - priority list-2026/5/13
2026-05-14查看详情 > -
Page: List of medicines under additional monitoring-2026/6/25
2026-06-26查看详情 > -
Studying Multiple Versions of a Cellular or Gene Therapy Product in an Early-Phase Clinical Trial (Final)-2022/11/4
2022-11-30查看详情 > -
Guidance for industry to prevent and mitigate medicine shortages-2023/5/17
2023-05-18查看详情 > -
国家药监局关于修订风寒感冒颗粒、穿心莲注射液药品说明书的公告(2023年第139号)-2023/11/22
2023-11-23查看详情 > -
Document: Policy 83: Policy on visiting and collaborating experts involved in the activities of the European Medicines Agency-2025/1/17
2025-01-20查看详情 > -
Document: Minimum inhibitory concentration (MIC) breakpoints-2025/2/21
2025-02-24查看详情 > -
Document: Concept paper on the revision of the guideline on the Scientific Data Requirements for a Plasma Master File (PMF) Revision 1 and Annexes-2025/3/31
2025-04-01查看详情 >