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ÇѱÛÁ¦¸ñ(Korean Title) |
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¿µ¹®Á¦¸ñ(English Title) |
Development Life Cycle-Based Association Analysis of Requirements for Risk Management of Medical Device Software |
ÀúÀÚ(Author) |
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DongYeop Kim
Ye-Seul Park
Jung-Won Lee
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¿ø¹®¼ö·Ïó(Citation) |
VOL 06 NO. 12 PP. 0543 ~ 0548 (2017. 12) |
Çѱ۳»¿ë (Korean Abstract) |
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¿µ¹®³»¿ë (English Abstract) |
In recent years, the importance of the safety of medical device software has been emphasized because of the function and role of the software among components of the medical device, and because the operation of the medical device software is directly related to the life and safety of the user. To this end, various standards have been set up that provide activities that can effectively ensure the safety of medical devices and provide their respective requirements. The activities that standards provide to ensure the safety of medical device software are largely divided into the development life cycle of medical device software and the risk management process. These two activities should be concurrent with the development process, but there is a limitation that the risk management requirements to be performed at each stage of the medical device software development life cycle are not classified. As a result, developers must analyze the association of standards directly to develop risk management activities during the development of medical devices. Therefore, in this paper, we analyze the relationship between medical device software development life cycle and risk management process, and extract risk management requirement items. It enables efficient and systematic risk management during the development of medical device
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Å°¿öµå(Keyword) |
°³¹ß»ý¸íÁÖ±â
ÀÇ·á±â±â ¼ÒÇÁÆ®¿þ¾î
ÀÇ·á±â±â À§Çè°ü¸®
Ç׸ñ ¿¬°ü¼º ºÐ¼®
Development Life Cycle
Medical Device Software
Medical Device Risk Management
Item Relevance Analysis
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