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国家药监局药审中心关于发布《真实世界证据支持药物注册申请的沟通交流指导原则（试行）》的通告（2023年第6号）-2023/02/16
2023-02-16查看详情 > -
2022年度药品审评报告-2023/9/6
2023-09-07查看详情 > -
Guidance for Industry: Questions and Answers Regarding Food Allergen Labeling (Edition 5)-20251/6
2025-01-07查看详情 > -
Page: Careers-2025/2/6
2025-02-10查看详情 > -
Document: PhV non-compliance notification contact points at National Competent Authority (NCA) level-2025/3/14
2025-03-17查看详情 > -
Document: Minutes of the CVMP meeting 11-13 March 2025-2025/4/16
2025-04-16查看详情 > -
Document: Draft European Union herbal monograph on Ononis spinosa L., radix - Revision 1-2025/6/2
2025-06-03查看详情 > -
Document: Combined Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) list of clinical terms for reporting suspected adverse events in animals and humans to veterinary medicinal products - Rev.16-2025/7/3
2025-07-04查看详情 > -
Document: Feedback from European Medicine Agency (EMA) to the EU Commission request to evaluate the feasibility of alternatives to replace titanium dioxide (TiO2) in medicinal products and its possible impact on medicines’ availability-2025/8/6
2025-08-07查看详情 > -
Document: List of medicinal products under additional monitoring-2025/9/24
2025-09-25查看详情 >
