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ISO 15198:2004
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Clinical laboratory medicine -- In vitro diagnostic medical devices -- Validation of user quality control procedures by the manufacturer

This standard was last reviewed* in 2008.

*ISO standards are reviewed every five years.

Abstract

ISO 15198:2004 describes a process for manufacturers of in vitro diagnostic medical devices to validate quality control procedures they recommend to their users. These quality control procedures are intended to provide users with assurance that device performance is consistent with its intended use and the manufacturers' claims. ISO 15198:2004 applies to all in vitro diagnostic medical devices.

 

  • Edition: 1 (Monolingual) ICS: 11.100.10
    Status: Published Stage: 90.60 (2013-09-18)
    TC/SC: ISO/TC 212 Number of Pages: 10
  • No revision information available

  • No corrigenda or amendments available

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