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Transfer of a Premarket Notification (510(k)) Clearance – Questions and Answers-2025/6/5
2025-06-06查看详情 > -
Page: Artificial intelligence-2025/7/10
2025-07-11查看详情 > -
药你知道 | 《国家药监局关于发布优化全生命周期监管支持高端医疗器械创新发展有关举措的公告》系列解读（四）-2025/8/20
2025-08-21查看详情 > -
Document: Draft guideline on clinical investigation of medicinal products for the treatment of psoriatic arthritis - Revision 1-2025/9/30
2025-10-08查看详情 > -
国家药监局关于优化境外生产药品补充申请审评审批程序试点工作的通知-2025/11/7
2025-11-10查看详情 > -
Page: Medicines for human use under evaluation-2025/12/5
2025-12-08查看详情 > -
Page: Medicine evaluation figures-2026/1/15
2026-01-16查看详情 > -
Page: Clinical Pharmacology Operational Expert Group-2026/2/16
2026-02-26查看详情 > -
Document: Request/declaration form for the provision of information via mobile scanning and other technologies in the centralised procedure-2026/3/25
2026-03-26查看详情 > -
Page: ICH Q3C (R9) Residual solvents - Scientific guideline-2026/4/29
2026-04-30查看详情 >
