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¿µ¹® Ç¥Áظí Requirement Specification of Information EOL Management System in Pharmaceutical Industry
ÇÑ±Û ³»¿ë¿ä¾à º» Ç¥ÁØÀº Á¦¾à»ê¾÷ °ø±Þ¸Á Àü ´Ü°è¿¡¼­ ¹ß»ýÇÏ´Â °³º°º¸°ü Á¤º¸, »óÈ£±³È¯ Á¤º¸ ¹× ±â°üº¸°í Á¤º¸¿¡ ´ëÇØ¼­ º¸Á¸±â°£ÀÌ ¸¸·áµÈ Á¤º¸µéÀ» ½Äº°Çϰí, ÀûÀýÈ÷ Æó±âÇϸç À̸¦ ½Ã½ºÅÛÈ­ Çϱâ À§ÇÏ¿© PDCA (Plan-Do-Check-Act) °ü¸® »çÀÌŬ¿¡ ÀÔ°¢ÇÑ Æó±â´ë»ó Á¤º¸(Information EOL) °ü¸®½Ã½ºÅÛ Ç¥ÁØÀÌ´Ù.
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¿µ¹® ³»¿ë¿ä¾à This technical report specifies information EOL (End Of Life) management system requirements based on PDCA (Plan-Do-Check-Act) management cycle. The target information of this system are individual information, exchanging information and reporting information over the whole pharmaceutical industry. This technical report mentions about followings:
․ Planning of Information EOL disposal
․ Execution of Information EOL disposal
․ Validation of Information EOL disposal
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°ü·ÃÆÄÀÏ  TTAR-06.0092.zip
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Á¦¾à»ê¾÷ Æó±â´ë»ó Á¤º¸ °ü¸®½Ã½ºÅÛ ¿ä±¸»çÇ× (±â¼úº¸°í¼­) TTAR-06.0092 2011-05-25 Á¦Á¤ ÆóÁö ¾øÀ½
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