Norm

NEN-EN-ISO 20186-2:2019 en

Moleculair in vitro diagnostisch onderzoek - Specificatie voor de pre-onderzoeksprocessen voor veneus heel bloed - Deel 2: Geïsoleerd genomisch DNA

118,48 129,14 Incl BTW

Over deze norm

Status Definitief
Aantal pagina's 20
Commissie In vitro diagnostica
Gepubliceerd op 01-04-2019
Taal Engels
NEN-EN-ISO 20186-2 gives guidelines on the handling, storage, processing and documentation of venous whole blood specimens intended for genomic DNA 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 DNA, which are not described in this document. Abstract national

Details

ICS-code 11.100.10
Nederlandse titel Moleculair in vitro diagnostisch onderzoek - Specificatie voor de pre-onderzoeksprocessen voor veneus heel bloed - Deel 2: Geïsoleerd genomisch DNA
Engelse titel Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated cellular RNA
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