[1]赖锦坝,李小江,张龚敏.医疗器械软件质量技术标准研究[J].医学信息,2019,(07):30-32.[doi:10.3969/j.issn.1006-1959.2019.07.011]
 LAI Jin-ba,LI Xiao-jiang,ZHANG Gong-min.Discussion On the Quality and Technical Standards of Medical Device Software[J].Medical Information,2019,(07):30-32.[doi:10.3969/j.issn.1006-1959.2019.07.011]
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医疗器械软件质量技术标准研究()
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医学信息[ISSN:1006-1959/CN:61-1278/R]

卷:
期数:
2019年07期
页码:
30-32
栏目:
医学信息学
出版日期:
2019-04-01

文章信息/Info

Title:
Discussion On the Quality and Technical Standards of Medical Device Software
文章编号:
1006-1959(2019)07-0030-03
作者:
赖锦坝李小江张龚敏
(广东省药品监督管理局审评认证中心,广东 广州 510080)
Author(s):
LAI Jin-baLI Xiao-jiangZHANG Gong-min
(Center For Certification and Evaluation,Guangdong Food And Drug Administration,Guangzhou510080,Guangdong,China)
关键词:
医疗器械软件质量技术标准
Keywords:
Medical equipmentSoftware qualityTechnical standards
分类号:
TP31;R197.39
DOI:
10.3969/j.issn.1006-1959.2019.07.011
文献标志码:
B
摘要:
基于现阶段医疗器械法规的要求,对医疗器械软件合规性、类别,文档的完整性、系统的标准性及临床的有效性等进行探讨。医疗器械软件制造商需强化法规要求,将医疗器械法规要求融入软件技术标准中,持续改进产品,保证医疗器械软件质量,确保医疗器械产品的安全性、有效性。
Abstract:
Based on the requirements of current medical device regulations, medical device software compliance, categories, document integrity, system standardization and clinical effectiveness are discussed. Medical device software manufacturers need to strengthen regulatory requirements, integrate medical device regulatory requirements into software technology standards, continuously improve products, ensure the quality of medical device software, and ensure the safety and effectiveness of medical device products.

参考文献/References:


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更新日期/Last Update: 2019-04-01