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Ȩ Ȩ > ¿¬±¸¹®Çå > ±¹³» ³í¹®Áö > Çѱ¹Á¤º¸°úÇÐȸ ³í¹®Áö > Á¤º¸°úÇÐȸ³í¹®Áö (Journal of KIISE)

Á¤º¸°úÇÐȸ³í¹®Áö (Journal of KIISE)

Current Result Document :

ÇѱÛÁ¦¸ñ(Korean Title) ÀΰøÁö´É ÀÇ·á±â±â ¼ÒÇÁÆ®¿þ¾îÀÇ IEC 62304 ±¹Á¦Ç¥ÁØ Áؼö °¡À̵å¶óÀÎ °³¹ß ¹× Àû¿ë
¿µ¹®Á¦¸ñ(English Title) Development and Application of Guidelines for Compliance with IEC 62304 International Standards for AI Medical Device Software
ÀúÀÚ(Author) ±èµ¿¿±   ¹Ú¿¹½½   À̺´Á¤   ÀÌÁ¤¿ø   DongYeop Kim   Ye-Seul Park   Byungjeong Lee   Jung-Won Lee  
¿ø¹®¼ö·Ïó(Citation) VOL 48 NO. 01 PP. 0071 ~ 0081 (2021. 01)
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(Korean Abstract)
ÀÇ·á±â±â ¼ÒÇÁÆ®¿þ¾î °³¹ßÀÚ´Â ÀÇ·á±â±â ¼ÒÇÁÆ®¿þ¾î »ý¸íÁÖ±â ÇÁ·Î¼¼½º¿¡ ´ëÇÑ ±¹Á¦Ç¥ÁØÀÎ IEC 62304°¡ ¿ä±¸ÇÏ´Â ÇÁ·Î¼¼½º¸¦ ¼ö¸³ÇÏ°í, ¹æ´ëÇÑ ¾çÀÇ »êÃâ¹°À» °®Ãß¾î ÀÎÇã°¡¸¦ ¹Þ¾Æ¾ß ÇÑ´Ù. ÃÖ±Ù¿¡ ´Â ÀǷ῵»ó ±â¹Ý ÀΰøÁö´É ÀÇ·á±â±â ¼ÒÇÁÆ®¿þ¾î°¡ È°¹ßÈ÷ °³¹ßµÇ°í ÀÖÀ¸¸ç, µ¶¸³Çü ¼ÒÇÁÆ®¿þ¾î·Î Ãë±ÞµÇ±â ¶§¹®¿¡ ÀÇ·á±â±â ¼ÒÇÁÆ®¿þ¾î¿¡ ´ëÇÑ IEC 62304¸¦ ÁؼöÇÏ¿© ÀÎÇã°¡¸¦ ¹Þ¾Æ¾ß ÇÑ´Ù. ÀΰøÁö´É ±â¼ú¿¡ ´ëÇÑ ±¹Á¦Ç¥ÁØÀº ³íÀÇ ´Ü°è¿¡ ÀÖ¾î, °³¹ßÀÚ´Â ÀΰøÁö´É ÀÇ·á±â±â ¼ÒÇÁÆ®¿þ¾îÀÇ »ý¸íÁÖ±â ÇÁ·Î¼¼½º¸¦ ÀÓÀÇ·Î ¼ö¸³ÇØ¾ß Çϸç, IEC 62304ÀÇ ¾î´À ¸í¼¼¸¦ ±âÁØÀ¸·Î »ï¾Æ ÀΰøÁö´É Á¦Ç°ÀÇ ¼º´É°ú ¾ÈÀü¼ºÀ» ÀÔÁõÇÒÁö, ¾î¶² Ç°Áú°ü¸® ±â¹ýÀ» »ç¿ëÇÏ¿© »êÃâ¹°À» ÀÛ¼ºÇÒÁö ÆľÇÇϱ⠾î·Æ´Ù. º» ³í¹®Àº ÀΰøÁö´É ÀÇ·á±â±â ¼ÒÇÁÆ®¿þ¾î¿¡ ´ëÇÑ IEC 62304 Áؼö ¹üÀ§¿Í ¿ä±¸»çÇ×À» ¼öÇàÇϱâ À§ÇÑ Ç°Áú°ü¸® ±â¹ýÀ» °¡À̵å¶óÀÎÀÇ ÇüÅ·ΠÁ¦°øÇÑ´Ù. ¶ÇÇÑ ½ÇÁ¦ ÀΰøÁö´É Á¦Ç°¿¡ Àû¿ëÇÏ¿© º» °¡À̵å¶óÀÎÀÇ È°¿ë¼ºÀ» È®ÀÎÇÑ´Ù.
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(English Abstract)
Medical device software developers must implement the processes required by IEC 62304, the international standard for medical device software life-cycle processes, and they must also have a large amount of artifacts to obtain a license. Recently, AI medical device software based on medical images has been actively developed, and since it is treated as standalone software, it must be approved in accordance with IEC 62304 for medical device software. The international standard for AI technology is currently in the discussion stage, and the developer should arbitrarily establish the life-cycle process of AI medical device software, and by matching the specifications of IEC 62304, the performance and safety of AI products will be evaluated. It is unclear which quality management technique should be used to produce the best artifact. This paper provides a quality control technique for fulfilling the scope and requirements of IEC 62304 compliance for AI medical device software in the form of guidelines. These guidelines are also applied to actual AI products to check their potential use in real applications.
Å°¿öµå(Keyword) ÀΰøÁö´É   ÀÇ·á±â±â ¼ÒÇÁÆ®¿þ¾î   IEC 62304   ±¹Á¦Ç¥ÁØ   artificial intelligence   medical device software   IEC 62304   international standard  
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