CEN/TS 17305:2019

Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA CEN/TS 17305:2019

Publication date:   Aug 15, 2019

General information

99.60   Withdrawal effective   Nov 3, 2021

CEN

CEN/TC 140 In vitro diagnostic medical devices

Technical Specification

11.100.10   In vitro diagnostic test systems

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Scope

This document gives requirements on the handling, storage, processing and documentation of saliva specimens intended for human DNA examination during the pre-examination phase before a molecular examination is performed.
This document is applicable to molecular in vitro diagnostic examination including laboratory developed tests performed by medical laboratories. It is also intended to be used by laboratory customers, in vitro diagnostics developers and manufacturers, biobanks, institutions and commercial organisations performing biomedical research, and regulatory authorities.
Dedicated measures that need to be taken for saliva collected on absorbing material or by mouth washes are not described in this technical specification. Neither are measures for preserving and handling of native saliva cell-free DNA, pathogens, and other bacterial or whole microbiome DNA in saliva described.
NOTE International, national or regional regulations or requirements can also apply to specific topics covered in this document.

Life cycle

NOW

WITHDRAWN
CEN/TS 17305:2019
99.60 Withdrawal effective
Nov 3, 2021

REVISED BY

PUBLISHED
EN ISO 4307:2021




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