ISO/DTS 21385

This draft is in the approval phase.

Abstract

This document provides general requirement and guidance on identification, design and development of emerging technologies with potential use in medical laboratories and their preparation for clinical use. This document is applicable to laboratories transitioning emerging technologies utilizing human samples into medical laboratory examinations for the purpose of providing information for the diagnosis, monitoring, management, prevention, and treatment of disease. This document does not apply to medical laboratory examinations undergoing validation at which point the technology has become an in-house (laboratory developed) test or in-vitro diagnostic medical device.

General information

Status
: Under development

Stage
: Final text received or FDIS registered for formal approval [50.00]
Edition
: 1

Number of pages
: 29
Technical Committee :
ISO/TC 212

ICS :
11.100.01
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