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About This Item

 

Full Description

This document describes the particular clinical laboratory practice requirements to ensure the quality of detection, identification and quantification of microbial pathogens using nucleic acid amplification tests (NAAT).

All current amendments available at time of purchase are included with the purchase of this document.
 

Document History

  1. BS ISO 17822:2020

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    In vitro diagnostic test systems. Nucleic acid amplification-based examination procedures for detection and identification of microbial pathogens. Laboratory quality practice guide

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  2. BS PD ISO/TS 17822-1:2014


    <i>In</i> <i>vitro</i> diagnostic test systems. Qualitative nucleic acid-based <i>in</i> <i>vitro</i> examination procedures for detection and identification of microbial pathogens-General requirements, terms and definitions

    • Historical Version