首页 >
法规速递
-
Document: Minutes of the CVMP meeting 3-5 December 2024-2025/1/24
2025-02-05查看详情 > -
Document: Infographic - Orphan Medicines in the EU-2025/2/27
2025-03-03查看详情 > -
国家药监局关于进一步做好《药品生产许可证》发放有关事项的公告（2025年第35号）-2025/4/7
2025-04-08查看详情 > -
Document: Annex - National provisions for SMEs applicable to the pharmaceutical sector-2025/5/15
2025-05-16查看详情 > -
六部门联合发布《关于将4-哌啶酮和1-叔丁氧羰基-4-哌啶酮列为易制毒化学品管理的公告》-2025/6/25
2025-06-26查看详情 > -
Document: Key elements form: Applicant’s proposal for a paediatric-investigation-plan opinion-2025/7/28
2025-07-29查看详情 > -
国家药监局关于莲芝消炎软胶囊和肾骨片转换为非处方药的公告（2025年第84号） -2025/9/12
2025-09-12查看详情 > -
Document: Minutes of the CVMP meeting 9-10 September 2025-2025/10/17
2025-10-17查看详情 > -
国家药监局综合司关于印发《药用辅料附录检查指导原则》《药包材附录检查指导原则》的通知-2025/11/21
2025-11-24查看详情 > -
Study of Sex Differences in the Clinical Evaluation of Medical Products-2025/12/15
2025-12-16查看详情 >
