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>UNE EN ISO 20166-1:2019 - Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 1: Isolated RNA (ISO 20166-1:2018)
sklademVydáno: 2019-10-23
UNE EN ISO 20166-1:2019 - Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 1: Isolated RNA (ISO 20166-1:2018)

UNE EN ISO 20166-1:2019

Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 1: Isolated RNA (ISO 20166-1:2018)

Examen de diagnóstico molecular in vitro. Especificaciones para los procesos preanalíticos para tejido fijado en formol e incluido en parafina (FFPE). Parte 1: ARN aislado. (ISO 20166-1:2018).

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Označení normy:UNE EN ISO 20166-1:2019
Počet stran:31
Vydáno:2019-10-23
Status:Norma
Počet stran (Španělsky):32
DESCRIPTION

UNE EN ISO 20166-1:2019

This International Standard recommends the handling, documentation, storage and processing of formalin-fixed and paraffin-embedded (FFPE) tissue specimens intended for RNA examination during the pre-examination phase before a molecular assay is performed. This International Standard 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, as well as institutions and commercial organizations performing biomedical research, biobanks, and regulatory authorities. The formalin-fixation and the paraffin-embedding process lead to modifications of the RNA molecules, which can impact the validity and reliability of the examination test results. RNA profiles in tissues can change drastically during collection and change differently in different tissue donors / patients tissues. Therefore, it is essential to take special measures to minimize the described RNA profile changes and modifications within the tissue for subsequent examination. NOTE International, national or regional regulations or requirements may also apply to specific topics covered in this International Standard.

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