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ILNAS-EN ISO 20166-3:2019 Edition 01/2019
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 3: Isolated DNA (ISO 20166-3:2018)
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Abstract

This document gives guidelines on the handling, documentation, storage and processing of formalin-fixed and paraffin-embedded (FFPE) tissue specimens intended for DNA examination during the pre-examination phase before a molecular assay is performed. This document is applicable to molecular in vitro diagnostic examinations including laboratory developed tests performed by medical laboratories and molecular pathology 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. NOTE International, national or regional regulations or requirements can also apply to specific topics covered in this document.

Status

Standard - Active

Origin

Technical Committee :
CEN/TC 140 : In vitro diagnostic medical devices

Implementation

start of the vote on the project    30/06/2016   date of ratification (dor)    21/12/2018
end of the vote on the project    20/09/2016   date of anouncement (doa)    30/04/2019
start of the vote on the final project    27/09/2018   date of publication (dop)    31/07/2019
end of the vote on the final project    20/11/2018   date of withdrawal (dow)    31/01/2022


Publication Official Journal
of the Grand-Duchy of Luxembourg
13/02/2019
Reference Mémorial A N° 65

Relations

Relations to older standards
CEN/TS 16827-3:2015

Relations to international standards
ISO 20166-3 
ISO 20166-3:2018 

International Classification for Standards (ICS codes) :

11.100.10 : In vitro diagnostic test systems

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