ISO15198
Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturer
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.
This document is available in electronic only.
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{{FormatPrice(nonMemberPrice)}} List PriceISO 15198: Clinical Laboratory Medicine - In Vitro Diagnostic Medical Devices - Validation of User Quality Control Procedures by the Manufacturer.
Organization: ISO
Date of Publication: 03/20/2004
Edition: First Edition
Pages: 10
ISO 15198: Clinical Laboratory Medicine - In Vitro Diagnostic Medical Devices - Validation of User Quality Control Procedures by the Manufacturer.
Organization: ISO
Date of Publication: 03/20/2004
Edition: First Edition
Pages: 10