{"id":599419,"date":"2024-11-05T22:01:05","date_gmt":"2024-11-05T22:01:05","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/iso-175932007\/"},"modified":"2024-11-05T22:01:05","modified_gmt":"2024-11-05T22:01:05","slug":"iso-175932007","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/iso\/iso-175932007\/","title":{"rendered":"ISO 17593:2007"},"content":{"rendered":"

ISO 17593:2007 specifies requirements for in vitro<\/i> measuring systems for self-monitoring of vitamin-K antagonist therapy, including performance, quality assurance and user training and procedures for the verification and validation of performance by the intended users under actual and simulated conditions of use. <\/p>\n

ISO 17593:2007 pertains solely to prothrombin time measuring systems used by individuals for monitoring their own vitamin-K antagonist therapy, and which report results as international normalized ratios (INR). <\/p>\n

ISO 17593:2007 is applicable to manufacturers of such systems and those other organizations (e.g., regulatory authorities and conformity assessment bodies) having the responsibility for assessing the performance of these systems.<\/p>\n

ISO 17593:2007 does not<\/p>\n