International Standard
ISO 17822:2020
In vitro diagnostic test systems — Nucleic acid amplification-based examination procedures for detection and identification of microbial pathogens — Laboratory quality practice guide
Reference number
ISO 17822:2020
Edition 1
2020-11
International Standard
Read sample
ISO 17822:2020
67022
Published (Edition 1, 2020)

ISO 17822:2020

ISO 17822:2020
67022
Language
Format
CHF 173
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Abstract

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).

It is intended for use by laboratories that develop, and/or implement and use, or perform NAAT for medical, research or health-related purposes. This document does not apply to the development of in vitro diagnostic (IVD) medical devices by manufacturers. However, it does include verification and validation of such devices and/or the corresponding processes when implemented and used by the laboratories.

General information

  •  : Published
     : 2020-11
     : 2020-12
    : International Standard published [60.60]
  •  : 1
     : 39
  • ISO/TC 212
    11.100.01 
  • RSS updates

Sustainable Development Goals

This standard contributes to the following Sustainable Development Goal

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