首页 >
法规速递
-
Draft Guidance: Formal Meetings Between the FDA and Sponsors or Applicants of PDUFA Products-2023/9/21
2023-09-22查看详情 > -
Document: Work plan for the Committee for Veterinary Medicinal Products (CVMP) Efficacy Working Party (EWP-V) 2025-2025/1/6
2025-01-07查看详情 > -
Document: Jakavi-H-C-002464-X-0070-G : EPAR - Assessment report - Variation-2025/2/11
2025-02-12查看详情 > -
关于公开征求《化学仿制药参比制剂目录(第九十二批)》(征求意见稿)意见的通知-2025/3/19
2025-03-20查看详情 > -
Document: Business process description for scientific meeting management-2025/4/22
2025-04-23查看详情 > -
Document: Faecal microbiota transplantation EU-IN Horizon Scanning Report-2025/6/2
2025-06-03查看详情 > -
Document: Dates of 2026 Scientific Advice Working Party (SAWP) meetings and submission deadlines for scientific advice, protocol assistance, qualification of novel methodologies and HTACG/EMA parallel Joint Scientific Consultation (JSC) requests-2025/7/8
2025-07-09查看详情 > -
Document: Combined VeDDRA list of clinical terms for reporting suspected adverse events in animals and humans to veterinary medicinal products-2025/8/12
2025-08-13查看详情 > -
药你知道 | 《国家药监局关于发布优化全生命周期监管支持高端医疗器械创新发展有关举措的公告》系列解读(八)-2025/9/26
2025-09-28查看详情 > -
Document: Member states contact points for review of national versions of the content of mobile scanning and other technologies-2025/11/4
2025-11-05查看详情 >