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Document: Annex to 16-19 June 2025 CHMP Minutes-2026/2/10
2026-02-11查看详情 > -
Document: QRD veterinary Appendix I - Adverse event (PhV) MSs reporting details-2026/3/19
2026-03-20查看详情 > -
2026年4月24日中药品种保护受理公示-2026/4/24
2026-04-27查看详情 > -
国家药监局关于发布仿制药参比制剂目录（第六十一批）的通告（2022年第52号）-2022/10/20
2022-11-14查看详情 > -
Regulatory and procedural guideline: Guideline on computerised systems and electronic data in clinical trials-2023/03/10
2023-03-10查看详情 > -
Scientific guideline: Draft guideline on clinical investigation of medicinal products in the treatment of depression - Revision 3-2023/9/15
2023-09-15查看详情 > -
CVM GFI #251 - Heritable Intentional Genomic Alterations in Animals of Food-Producing Species for Use as Models of Disease-2025/1/7
2025-01-07查看详情 > -
Document: Members of the Coordinating group of European network of paediatric research at the European Medicines Agency (Enpr-EMA)-2025/2/10
2025-02-11查看详情 > -
Document: 2024-2026 Work Plan of the Good Clinical Practice Inspectors Working Group (GCP IWG)-2025/3/17
2025-03-18查看详情 > -
国家药监局 海关总署关于允许进口牛黄试点用于中成药生产有关事项的公告（2025年第25号）-2025/4/21
2025-04-22查看详情 >
