首页 >
法规速递
-
Document: European Medicines Agency’s data protection notice for the EMA Account Management system-2026/6/11
2026-06-12查看详情 > -
FDA and Industry Actions on Premarket Notification (510(k)) Submissions: Effect on FDA Review Clock and Goals(Final)-2022/10/3
2022-11-14查看详情 > -
国家药监局药审中心关于发布《抗肿瘤抗体偶联药物临床研发技术指导原则》的通告（2023年第25号）-2023/4/7
2023-04-10查看详情 > -
关于公开征求《化学药品注射剂配伍稳定性药学研究技术指导原则（征求意见稿）》意见的通知-2023/10/07
2023-10-08查看详情 > -
Document: EudraVigilance - EVWEB user manual-2025/1/7
2025-01-08查看详情 > -
Document: Agenda - EMA Veterinary Innovation Day - March 2025-2025/2/13
2025-02-14查看详情 > -
Document: PhV non-compliance notification contact points at National Competent Authority (NCA) level-2025/3/24
2025-03-25查看详情 > -
Page: CHMP opinions on consultation procedures-2025/4/24
2025-04-27查看详情 > -
Requests for Feedback and Meetings for Medical Device Submissions: The Q-Submission Program - Final Guidance for Industry and Food and Drug Administration Staff-2025/5/29
2025-06-06查看详情 > -
Document: 2024 AI Observatory report: Compilation of 2024 experience-2025/7/10
2025-07-11查看详情 >
