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Document: Dates of 2026 Scientific Advice Working Party - Human (SAWP-H) meetings and submission deadlines for scientific advice, protocol assistance, qualification of novel methodologies and HTACG/EMA parallel Joint Scientific Consultation (JSC) requests
2026-01-14查看详情 > -
Document: Medicine shortage communication (MSC): Natpar (parathyroid hormone) (25, 50, 75 and 100 micrograms/dose powder and solvent for solution for injection)-2026/2/13
2026-02-14查看详情 > -
Page: Guidance on good manufacturing practice and good distribution practice: Questions and answers-2026/3/24
2026-03-25查看详情 > -
Document: List of clinical evaluation consultation procedure (CECP) opinions issued for medical devices awaiting finalisation of conformity assessment-2026/4/28
2026-04-29查看详情 > -
Document: Records of data processing activity regarding EMA Account Management System (public)-2026/6/9
2026-06-10查看详情 > -
Document: Terms of reference for the European Medicines Agency – United States Food and Drugs Administration – Health Canada cluster on real world data-2026/7/17
2026-07-19查看详情 > -
关于公开征求《药物临床试验方案审评工作规范(征求意见稿)》意见的通知-2022/10/27
2022-11-14查看详情 > -
国家药监局关于发布化学仿制药参比制剂调整程序的公告(2023年第35号)-2023/03/24
2023-03-24查看详情 > -
Final Guidance: Human Prescription Drug and Biological Products--Labeling for Dosing Based on Weight or Body Surface Area for Ready-to-Use Containers--“Dose Banding”-2023/9/29
2023-10-07查看详情 > -
Document: Contact details of national competent authorities for requests to use a sticker to place the Unique Identifier on the outer/immediate packaging of centrally approved products-2025/1/7
2025-01-08查看详情 >