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Page: Post-authorisation measures: questions and answers-2026/3/27
2026-03-30查看详情 > -
Document: PDCO minutes of the 24-27 March 2026 meeting-2026/5/8
2026-05-09查看详情 > -
关于公开征求《抗肿瘤光动力治疗药物临床研发技术指导原则（征求意见稿）》意见的通知-2022/11/25
2022-11-25查看详情 > -
关于公开征求ICH《S12：基因治疗产品非临床生物分布的考虑》实施建议和中文版的通知-2023/4/28
2023-05-04查看详情 > -
关于公开征求《疫苗临床试验的统计学指导原则（征求意见稿）》意见的通知-2023/11/6
2023-11-07查看详情 > -
Document: Table of decisions of labelling exemption requests falling under article 63 of Directive 2001/83/EC examined by the Quality Review of Documents (QRD) Group-2025/1/15
2025-01-16查看详情 > -
国家药监局关于复方公英胶囊转换为非处方药的公告（2025年第17号）-2025/2/19
2025-02-21查看详情 > -
Evaluation of Sex-Specific Data in Medical Device Clinical Studies - Guidance for Industry and Food and Drug Administration Staff-2025/3/31
2025-04-01查看详情 > -
Document: European Medicines Agency policy on access to EudraVigilance data for medicinal products for human use - Revision 5-2025/5/5
2025-05-06查看详情 > -
Document: Organisation chart: Administration and Corporate Management-2025/6/16
2025-06-17查看详情 >
