首页 >
法规速递
-
CVM GFI #236 Clarification of FDA and EPA Jurisdiction Over Mosquito-Related Products-2025/8/27
2025-08-28查看详情 > -
Page: Other fees and charges for medicinal products for human use, veterinary medicinal products and consultations on medical devices-2025/10/2
2025-10-08查看详情 > -
国家药监局关于批准注册204个医疗器械产品的公告（2025年10月）（2025年第111号）-2025/11/11
2025-11-12查看详情 > -
Page: European Surveillance of Veterinary Antimicrobial Consumption (ESVAC): 2009 - 2023-2025/12/9
2025-12-10查看详情 > -
Document: Applications for new human medicines under evaluation: January 2026-2026/1/20
2026-01-21查看详情 > -
Document: Minutes of the CVMP meeting 13-15 January 2026-2026/2/20
2026-02-27查看详情 > -
Document: Clinical Trial Information System (CTIS) - Sponsor handbook-2026/3/26
2026-03-27查看详情 > -
Page: Quality of medicines: questions and answers - Part 2-2026/5/5
2026-05-06查看详情 > -
Document: Regulatory Procedure Management in IRIS roadmap-2026/6/16
2026-06-17查看详情 > -
Document: List of changes to combined Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) list of clinical terms for reporting suspected adverse events in animal and humans to veterinary medicinal products for 2025-2026/7/24
2026-07-26查看详情 >
