Search
×
FR

Placeholder headline

This is just a placeholder headline

TEMA 11th Edition – Book of Standards (Not for Resale)

$

0

BUY NOW

Placeholder headline

This is just a placeholder headline

ISO 22040-3:2025 Life cycle management of concrete structures — Part 3: Execution stage

$

125

BUY NOW

Placeholder headline

This is just a placeholder headline

ISO 2382-19:1989 Information processing systems — Vocabulary — Part 19: Analog computing

$

0

BUY NOW

Placeholder headline

This is just a placeholder headline

ISO 6490-1:1985 Animal feeding stuffs — Determination of calcium content — Part 1: Titrimetric method

$

82

BUY NOW

Placeholder headline

This is just a placeholder headline

ISO 8536-6:2025 Infusion equipment for medical use — Part 6: Freeze drying closures for infusion bottles

$

186

BUY NOW

Placeholder headline

This is just a placeholder headline

ISO 21702:2019 Measurement of antiviral activity on plastics and other non-porous surfaces

$

289

BUY NOW

ISO 18704:2026

ISO 18704:2026 Molecular in vitro diagnostic examinations — Requirements and recommendations for pre-examination processes for urine and other body fluids — Isolated cell-free DNA

CDN $251.00

This publication was last reviewed and confirmed in 2026.

Molecular in vitro diagnostic examinations — Requirements and recommendations for pre-examination processes for urine and other body fluids — Isolated cell-free DNA

Description

This document specifies requirements and provides recommendations for the pre-examination process of cell-free DNA (cfDNA) from body fluid specimens other than blood, including but not limited to the collection, handling, storage, transport, processing and documentation of human body fluids, such as urine, pleural effusions, ascites, cerebrospinal fluid (CSF), and saliva, intended for cfDNA examination. Processing includes multiple steps, such as centrifugation for specimen purification and isolation of cfDNA.

This document does not cover dedicated measures for cytohistological analysis of nucleated cells derived from body fluid, nor measures for preserving and handling of pathogens, and other bacterial or whole microbiome DNA in body fluids described.

Dedicated measures for preserving circulating cell-free DNA (ccfDNA) from blood are covered in ISO 20186-3.

This document is applicable to medical laboratories, health institutions including facilities collecting and handling specimens, laboratory customers, in vitro diagnostic examination developers and manufacturers, biobanks, institutions and 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.

Edition

1

Published Date

2026-06-19

Status

PUBLISHED

Pages

25

Language Detail Icon

English

Format Secure Icon

Secure PDF

Abstract

This document specifies requirements and provides recommendations for the pre-examination process of cell-free DNA (cfDNA) from body fluid specimens other than blood, including but not limited to the collection, handling, storage, transport, processing and documentation of human body fluids, such as urine, pleural effusions, ascites, cerebrospinal fluid (CSF), and saliva, intended for cfDNA examination. Processing includes multiple steps, such as centrifugation for specimen purification and isolation of cfDNA.

This document does not cover dedicated measures for cytohistological analysis of nucleated cells derived from body fluid, nor measures for preserving and handling of pathogens, and other bacterial or whole microbiome DNA in body fluids described.

Dedicated measures for preserving circulating cell-free DNA (ccfDNA) from blood are covered in ISO 20186-3.

This document is applicable to medical laboratories, health institutions including facilities collecting and handling specimens, laboratory customers, in vitro diagnostic examination developers and manufacturers, biobanks, institutions and 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.

Previous Editions

Can’t find what you are looking for?

Please contact us at: