首页 >
法规速递
-
Page: Veterinary medicine safety day-2026/4/8
2026-04-09查看详情 > -
关于公开征求《中药改良型新药研究技术指导原则（征求意见稿）》意见的通知-2023/01/06
2023-01-06查看详情 > -
Draft Guidance: Inborn Errors of Metabolism That Use Dietary Management: Considerations for Optimizing and Standardizing Diet in Clinical Trials for Drug Product Development-2023/7/11
2023-07-13查看详情 > -
Final Guidance: Revising ANDA Labeling Following Revision of the RLD Labeling Guidance for Industry-2024/1/24
2024-02-05查看详情 > -
Document: European Shortages Monitoring Platform (ESMP) User guide for national competent authorities-2025/1/29
2025-02-05查看详情 > -
Document: Frequently asked questions (FAQs): How to create, submit and withdraw a Clinical Trial Application - CTIS Training Programme - Module 10-2025/3/5
2025-03-06查看详情 > -
Page: ICH Guideline M13B on bioequivalence for immediate-release solid oral dosage forms - additional strengths biowaiver - Scientific guideline-2025/4/9
2025-04-11查看详情 > -
Page: Electronic product information (ePI)-2025/5/20
2025-05-21查看详情 > -
Antibacterial Therapies for Patients With an Unmet Medical Need for the Treatment of Serious Bacterial Diseases – Questions and Answers-2025/6/26
2025-06-27查看详情 > -
Page: List of medicines under additional monitoring-2025/7/30
2025-07-31查看详情 >
