CEN ISO/TS 22367:2010

Medical laboratories - Reduction of error through risk management and continual improvement (ISO/TS 22367:2008, including Cor 1:2009) CEN ISO/TS 22367:2010

Publication date:   Mar 22, 2010

General information

99.60 Withdrawal effective   Mar 11, 2020

CEN

CEN/TC 140 In vitro diagnostic medical devices

Technical Specification

11.100.01   Laboratory medicine in general

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Scope

ISO/TS 22367:2008 characterizes the application of ISO 15189 as a system for reducing laboratory error and improving patient safety by applying the principles of risk management, with reference to examination aspects, especially to pre- and post-examination aspects, of the cycle of laboratory medical care. ISO/TS 22367:2008 proposes a methodology for finding and characterizing medical laboratory error that would be avoided with the application of ISO 15189.

Life cycle

NOW

WITHDRAWN
CEN ISO/TS 22367:2010
99.60 Withdrawal effective
Mar 11, 2020

REVISED BY

PUBLISHED
EN ISO 22367:2020

Relations

Adopted from ISO/TS 22367:2008 IDENTICAL