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I.S. EN ISO 20186-3:2019&LC:2019

Current

Current

The latest, up-to-date edition.

Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma (ISO 20186-3:2019)

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

10-11-2019

For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.

Only cited Standards give presumption of conformance to New Approach Directives/Regulations.


Dates of withdrawal of national standards are available from NSAI.

€37.00
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Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 General consideration
5 Outside the laboratory
6 Inside the laboratory
Annex A (informative) Impact of pre-examination process steps on circulating cell free DNA profiles in venous whole blood plasma
Bibliography

This document provides recommendations and requirements on the handling, storage, processing and documentation of venous whole blood specimens intended for circulating cell free DNA (ccfDNA) examination during the pre-examination phase before an analytical test is performed.

Committee
TC 212
DevelopmentNote
CORRECTED VERSION IS NOW AVAILABLE
DocumentType
Standard
Pages
0
ProductNote
The date of any NSAI previous adoption may not match the date of its original CEN/CENELEC document.
CORRECTED VERSION IS NOW AVAILABLE
PublisherName
National Standards Authority of Ireland
Status
Current

Standards Relationship
ISO 20186-3:2019 Identical
EN ISO 20186-3:2019 Identical

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