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prDS CEN ISO/TS 7552-1:2024

Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumour cells (CTCs) in venous whole blood - Part 1: Isolated RNA (ISO/TS 7552-1:2024)

General information

40.20     Feb 10, 2025

40.60    May 6, 2025

DPS

DPS/KT 140

Technical Specification

11.100.10  

Scope

This document specifies requirements and gives recommendations on the handling, storage, CTC enrichment and isolation, RNA isolation and storage, and documentation of venous whole blood specimens intended for the examination of RNA isolated from circulating tumour cells (CTCs) during the pre-examination phase before a molecular examination is performed.
This document is applicable to molecular in vitro diagnostic examinations 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 organizations performing biomedical research, and regulatory authorities.
This document does not cover the isolation of cellular RNA directly from venous whole blood containing CTCs. This is covered in ISO 20186-1.
This document does not cover the isolation of specific white blood cells and subsequent isolation of cellular RNA therefrom. This document does not cover pre-analytical workflow requirements for viable CTC cryopreservation and culturing.
NOTE 1        The requirements given in this document can also be applied to other circulating rare cells (e.g. foetal cells).
NOTE 2        International, national or regional regulations or requirements can also apply to specific topics covered in this document.

Life cycle

PREVIOUSLY

PUBLISHED
DS CEN/TS 17390-1:2020

NOW

IN_DEVELOPMENT
prDS CEN ISO/TS 7552-1:2024
40.20 DIS ballot initiated: 12 weeks
Feb 10, 2025

Related project

Adopted from CEN ISO/TS 7552-1:2024 IDENTICAL

Adopted from ISO/TS 7552-1:2024 IDENTICAL

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