ISO 17593:2007
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Clinical laboratory testing and in vitro medical devices -- Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy

This standard was last reviewed* in 2011.

*ISO standards are reviewed every five years.


ISO 17593:2007 specifies requirements for in vitro 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.

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).

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.

ISO 17593:2007 does not

  • pertain to in vitro measuring systems for coagulation quantities assessing vitamin-K antagonist therapy used by physicians or healthcare providers,
  • provide a comprehensive evaluation of all possible factors that could affect the performance of these systems, or
  • address the medical aspects of oral anticoagulation therapy.


  • Document published on: 2007-04-15
    Edition: 1 (Monolingual) ICS: 11.100.20
    Status: Published Stage: 90.93 (2011-10-19)
    TC/SC: ISO/TC 212 Number of Pages: 54
  • No revision information available

  • No corrigenda or amendments available

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