fig. beginning
Success Stories
Our Advantages
Project experience
Key Cases
Information Regulations
Prospect Research Space
Medical Device Safety Alert Opinion
Domestic Medical Device Safety Alert Opinion
Overseas Medical Device Safety Alert Opinion
New legislation, interpretation, guidelines
inquiry system
Catalog of Medical Devices Exempted from Clinical Evaluation (2023)
Medical Device Classification Catalog Search (Current)
Service Programs
About Us
English
简体中文
Español
Français
Русский
العربية
Português
Guangzhou Run Nan Zhi Information Technology Co.
Home
Information Regulations
Prospect Research Space
China's medical device unique identification UDI application analysis and outlook
Prospect Research Space
,
Information Regulations
2025年3月8日 pm6:13
相关新闻
再生元:双AAV基因疗法使遗传性耳聋患者恢复听力
百多力股份有限公司BIOTRONIK AG对自膨式镍钛合金外周血管支架系统主动召回 (2025-02-25)
93%患者达到主要疗效终点,新机制疗法已展开3期临床试验
The State Drug Administration (SDA) has issued new regulations on the supervision and management of medical devices!
Announcement of the State Drug Administration on Further Strengthening the Supervision and Management of Entrusted Manufacturing by Registrants of Medical Devices (No. 38 of 2024)
Boehringer Ingelheim: PDE4B Inhibitor IPF Successful in Second Phase III Clinic, to Submit Marketing Application
FDA clarifies policies for compounders as national GLP-1 supply begins to stabilize
Notice of the Establishment of the Medical Device Industry Standard "Medical Devices Using Brain-Computer Interface Technology Quality Requirements and Evaluation Methods for EEG Data Sets Used in Artificial Intelligence Algorithms" by the Comprehensive Department of the State Drug Administration (SDA)
Nearly half of patients achieved complete remission! Phase 3 Clinical Results of Roche's Breakthrough Therapy in New England Journal of Medicine
FDA approves potential "best-in-class" allozyme small molecule inhibitors
Contact Us
SHARE
TOP
简体中文
简体中文
Español
Français
Русский
العربية
Português
English
简体中文
简体中文
Español
Français
Русский
العربية
Português
English