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- ±â¹Ð¼º È®º¸: °³ÀÎ ÀÇ·áÁ¤º¸°¡ Çã°¡µÇÁö ¾ÊÀº »ç¶÷¿¡°Ô °ø°³µÇ°Å³ª, Çã°¡µÇÁö ¾ÊÀº ¿ëµµ·Î »ç¿ëµÇÁö ¾Ê°Ô ÇÕ´Ï´Ù. - ¹«°á¼º È®º¸: °³ÀÎ ÀÇ·áÁ¤º¸°¡ Çã°¡µÇÁö ¾ÊÀº ¹æ¹ýÀ¸·Î º¯È¯µÇ°Å³ª ÆÄ±«µÇÁö ¾Êµµ·Ï ÇÕ´Ï´Ù. - °¡¿ë¼º È®º¸: °³ÀÎ ÀÇ·áÁ¤º¸°¡ ½ÂÀÎµÈ »ç¿ëÀÚ¿¡°Ô´Â Áï½Ã Á¦°øµÇ¾î¾ß Çϸç, ÇÊ¿äÇÑ ¶§¿¡ ÇÊ¿äÇÑ °÷¿¡¼ ÇÊ¿äÇÑ ÇüÅ·ΠÁ¸ÀçÇϵµ·Ï ÇÕ´Ï´Ù.¾×Æ®´Â ÃÖ½ÅÀÇ »çÀ̹öº¸¾È ½ÃÇèÀÎÁõ¼ºñ½º¸¦ Á¦°øÇÕ´Ï´Ù.
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- ħÅõ½ÃÇè (Penetration Testing)
- ½ÇÁ¦ °ø°ÝÀÚÀÇ °üÁ¡¿¡¼ ½Ã½ºÅÛ¡¤¾ÖÇø®ÄÉÀ̼ǡ¤³×Æ®¿öÅ©¸¦ ´ë»óÀ¸·Î º¸¾È Ãë¾àÁ¡À» ã¾Æ³»°í, Ä§ÇØ °¡´É¼º°ú »ç¾÷ ¿µÇâµµ¸¦ °ËÁõÇÕ´Ï´Ù.
- ÆÛÁöÅ×½ºÆ® (Fuzz Testing)
- ÀԷ°ªÀ» ÀÚµ¿ »ý¼º¡¤º¯ÇüÇØ ÆÄ¼/ÇÁ·ÎÅäÄÝ/ÆÄÀÏ Ã³¸®¡¤ÀåÄ¡ ÀÎÅÍÆäÀ̽º¿¡¼ Å©·¡½Ã¡¤¸Þ¸ð¸® ¿À·ù¡¤¿¹¿Ü µ¿ÀÛÀ» ŽÁöÇÕ´Ï´Ù.
- Ãë¾à¼ºÆò°¡ (Vulnerability Assessment)
- ÀÚ»ê Àü¹Ý(¼¹ö¡¤¿£µåÆ÷ÀÎÆ®¡¤¾ÖÇø®ÄÉÀ̼ǡ¤³×Æ®¿öÅ©)ÀÇ º¸¾È ±¸¼º°ú ¾Ë·ÁÁø Ãë¾àÁ¡À» ü°èÀûÀ¸·Î ½Äº°¡¤Æò°¡ÇÕ´Ï´Ù.
- ÀÀ¿ëÇÁ·Î±×·¥ ¼Ò½ºÄÚµå ºÐ¼® (Secure Code Review)
- °³¹ß ÃʱâºÎÅÍ ¹èÆ÷ Àü±îÁö ÄÚµå ¼öÁØ¿¡¼ º¸¾È °áÇÔÀ» ¼±Á¦ÀûÀ¸·Î ã¾Æ, Ãë¾àÁ¡À» ¼öÁ¤ÇÒ ¼ö ÀÖµµ·Ï ÇÕ´Ï´Ù.
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- ÀÇ·á±â±â
- ¼ÒÇÁÆ®¿þ¾î(Æß¿þ¾î)¸¦ Æ÷ÇÔÇÏ´Â ÀÇ·á±â±â(SiMD)
- ¼ÒÇÁÆ®¿þ¾î ÀÇ·á±â±â(SaMD)
- ÇÁ·Î±×·¥ °¡´É ³í¸® Á¦¾î±â(PLC)¸¦ Æ÷ÇÔÇÏ´Â ÀÇ·á±â±â
- Á¤º¸Åë½Å±â±â/³×Æ®¿öÅ©Àåºñ
- ÄÄÇ»ÅÍ ¹× ¸ð¹ÙÀÏ ±â±â
- IoT ¹× ½º¸¶Æ® µð¹ÙÀ̽º
- »ê¾÷¿ë Á¦¾î ±â±â
- ÀÚµ¿Â÷ ¹× ¿î¼ÛÀåºñ
- IT ½Ã½ºÅÛ
- ±ÝÀ¶ ½Ã½ºÅÛ
- ÀÏ¹Ý ¼ÒºñÀÚ¿ë Á¦Ç°
°ü·Ã Àû¿ë±Ô°Ý
- ISO 14971 (Application of risk management to medical devices)
- IEC 62443-3-3 (System security requirements and security levels)
- IEC 62443-4-1 (Secure product development lifecycle requirements)
- IEC 62443-4-2 (Technical security requirements for IACS components)
- IEC 81001-5-1 (Health software and health IT systems safety, effectiveness and security - Part 5-1: Security - Activities in the product lifecycle)
- IEC TR 60601-4-5 (Medical electrical equipment – Part 4-5: Guidance and interpretation – Safety-related technical security specifications)
- IEC TR 80002-1 (Medical device software – Part 1: Guidance on the application of ISO 14971 to medical device software)
- ETSI EN 303 645 (Cyber Security for Consumer Internet of Things: Baseline Requirements)
- ANSI/AAMI SW96 (Standard For Medical Device Security - Security Risk Management For Device Manufacturers)
- UL 2900-1 (Software Cybersecurity for Network-Connectable Products, Part 1: General Requirements)
- EN 18031 (Common security requirements for radio equipment)
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¾×Æ®´Â Total Service¸¦ Á¦°øÇÕ´Ï´Ù.
STEP 01
- Á¢¼ö
- °í°´ÀÇ ½ÃÇè ¿äû¼¸¦ Á¢¼öÇÑ µÚ, Á¦Ç° Ư¼º°ú ´ë»ó ½ÃÇè ¹üÀ§¸¦ ¿¹ºñ Áø´ÜÇÕ´Ï´Ù.
STEP 02
- ¹®¼ °ËÅä ¹× ¹®¼È
- ÀÚü °³¹ßÇÑ ¹®¼ ÀÚµ¿È Ç÷§ÆûÀ» Ȱ¿ëÇØ ½Å¼ÓÇϰí ÀϰüµÈ ±â¼ú¹®¼ ÀÛ¼ºÀ» Áö¿øÇϸç, Á¦Ãâ ÀÚ·áÀÇ ¿Ï¼ºµµ¸¦ Á¡°ËÇÕ´Ï´Ù.
STEP 03
- Test Plan ¼ö¸³
- Á¦Ç°ÀÇ º¸¾È ¿ä±¸»çÇ×À» ±Ù°Å·Î ½ÃÇè°èȹ¼¸¦ ¼ö¸³Çϰí, ½ÃÇè ¹æ¹ý¡¤È¯°æ¡¤Æò°¡ ±âÁذú ¼¼ºÎ Ç׸ñÀ» ±¸Ã¼ÈÇÕ´Ï´Ù.
STEP 04
- ½ÃÇè½Ç½Ã
- ±¹³»¿Ü Ç¥ÁØ¿¡ ºÎÇÕÇϵµ·Ï Ãë¾àÁ¡ Áø´Ü, ¾ÏÈ£ ±â´É °ËÁõ, ³×Æ®¿öÅ©¡¤ÀÎÅÍÆäÀ̽º º¸¾È ½ÃÇè µî ´Ù¾çÇÑ Ç׸ñÀ» ¼öÇàÇÕ´Ï´Ù.
STEP 05
- ½ÃÇ輺Àû¼ ¹ß±Þ
- ½ÃÇè °á°ú¸¦ ÅëÇÕ ºÐ¼®ÇØ °´°üÀûÀÎ ½ÃÇè ¼ºÀû¼¸¦ ¹ßÇàÇÕ´Ï´Ù.
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- ±èÁÖ¿íº»ºÎÀå jw.kim@actslab.co.kr
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- ÀÓÀçÈﺻºÎÀå jh.im@actslab.co.kr