ISO/TS 22367:2008
Withdrawn
View Superseded by
Medical laboratories — Reduction of error through risk management and continual improvement
Hardcopy , PDF
04-24-2008
04-09-2025
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.
| Committee |
ISO/TC 212
|
| DocumentType |
Technical Specification
|
| Pages |
10
|
| PublisherName |
International Organization for Standardization
|
| Status |
Withdrawn
|
| SupersededBy |
| Standards | Relationship |
| NEN NPR CEN ISO/TS 22367 : 2010 | Identical |
| NEN NPR ISO/TS 22367 : 2008 C1 2009 | Identical |
| S.R. CEN ISO TS 22367:2010 | Identical |
| DD CEN ISO/TS 22367:2010 | Identical |
| CEN ISO/TS 22367:2010 | Identical |
| DIN ISO/TS 22367 : 2010 | Identical |
| DIN SPEC 1106;DIN ISO/TS 22367:2010-06 | Identical |
| DD ISO/TS 22367 : 2008 | Identical |
| BIS IS/ISO 15189 : 2012 | MEDICAL LABORATORIES - REQUIREMENTS FOR QUALITY AND COMPETENCE |
| I.S. EN ISO 15189:2012 | MEDICAL LABORATORIES - REQUIREMENTS FOR QUALITY AND COMPETENCE (ISO 15189:2012, CORRECTED VERSION 2014-08-15) |
| PREN ISO 15189 : DRAFT 2011 | MEDICAL LABORATORIES - PARTICULAR REQUIREMENTS FOR QUALITY AND COMPETENCE |
| 11/30173018 DC : 0 | BS EN ISO 15189 - MEDICAL LABORATORIES - PARTICULAR REQUIREMENTS FOR QUALITY AND COMPETENCE |
| DIN EN ISO 15189:2014-11 | Medical laboratories - Requirements for quality and competence (ISO 15189:2012, Corrected version 2014-08-15) |
| ISO 15189:2012 | Medical laboratories — Requirements for quality and competence |
| BS EN ISO 15189:2012 | Medical laboratories. Requirements for quality and competence |
| UNE-EN ISO 15189:2013 | Medical laboratories - Requirements for quality and competence (ISO 15189:2012, Corrected version 2014-08-15) |
| IEC 61025:2006 | Fault tree analysis (FTA) |
| IEC 60812:2006 | Analysis techniques for system reliability - Procedure for failure mode and effects analysis (FMEA) |
| ISO 15189:2012 | Medical laboratories — Requirements for quality and competence |
| AS ISO 22367:2021 | Medical laboratories - Application of risk management to medical laboratories |
| CLSI HS1 A2 : 2ED 2004 | A QUALITY MANAGEMENT SYSTEM MODEL FOR HEALTH CARE |
| ISO/IEC Guide 73:2002 | Risk management — Vocabulary — Guidelines for use in standards |
| ISO 9000:2015 | Quality management systems — Fundamentals and vocabulary |
| CLSI GP22 A2 : 2ED 2004 | CONTINUOUS QUALITY IMPROVEMENT: INTEGRATING FIVE KEY QUALITY SYSTEM COMPONENTS |
| ISO 14971:2007 | Medical devices — Application of risk management to medical devices |
| MIL-STD-1629 Revision A:1980 | PROCEDURES FOR PERFORMING A FAILURE MODE, EFFECTS AND CRITICALITY ANALYSIS (NO S/S DOCUMENT) |
| CLSI EP18 A : 1ED 2002 | QUALITY MANAGEMENT FOR UNIT-USE TESTING |
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