Reference number
ISO 20186-1:2019
International Standard
ISO 20186-1:2019
Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 1: Isolated cellular RNA
Edition 1
2019-02
Read sample
ISO 20186-1:2019
67217
Published (Edition 1, 2019)
This publication was last reviewed and confirmed in 2024. Therefore this version remains current.

ISO 20186-1:2019

ISO 20186-1:2019
67217
Language
Format
CHF 129
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Abstract

This document gives guidelines on the handling, storage, processing and documentation of venous whole blood specimens intended for cellular RNA examination during the pre-examination phase before a molecular examination is performed. This document covers specimens collected in venous whole blood collection tubes.

This document is applicable to any molecular in vitro diagnostic examination performed by medical laboratories. It is also intended to be used by laboratory customers, in vitro diagnostics developers and manufacturers, biobanks, institutions and commercial organizations performing biomedical research, and regulatory authorities.

Different dedicated measures are taken for stabilizing blood cell free circulating RNA and RNA in exosomes circulating in blood. These are not described in this document.

Different dedicated measures are taken for collecting, stabilizing, transporting and storing capillary blood as well as for collecting and storing blood by paper based technologies or other technologies generating dried blood. These are not described in this document.

This document does not cover the isolation of specific blood cells and subsequent isolation of cellular RNA therefrom.

RNA in pathogens present in blood is not covered by this document.

General information

  •  : Published
     : 2019-02
    : International Standard confirmed [90.93]
  •  : 1
     : 20
  • ISO/TC 212
    11.100.10 
  • RSS updates

Sustainable Development Goals

This standard contributes to the following Sustainable Development Goal

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