Clinical laboratory medicine -- In vitro diagnostic medical devices -- Validation of user quality control procedures by the manufacturer
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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.
Document published on: 2004-07-15 Edition: 1 (Monolingual) ICS: 11.100.10 Status: Published Stage: 90.60 (2013-09-18) TC/SC: ISO/TC 212 Number of Pages: 10
This standard has not been revised
No corrigenda or amendments available