CLSI EP18 A : 1ED 2002
Superseded
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
QUALITY MANAGEMENT FOR UNIT-USE TESTING
Superseded date
30-08-2007
Superseded by
Published date
12-01-2013
Publisher
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Covers quality management system for unit-use devices that will aid in the identification, understanding and management of sources of error and help to ensure correct results.
| DevelopmentNote |
Supersedes NCCLS EP18 P. (02/2003)
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| DocumentType |
Miscellaneous Product
|
| PublisherName |
Clinical Laboratory Standards Institute
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| Status |
Superseded
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| SupersededBy | |
| Supersedes |
| DD CEN ISO/TS 22367:2010 | Medical laboratories. Reduction of error through risk management and continual improvement |
| CLSI EP25 A : 1ED 2009 | EVALUATION OF STABILITY OF IN VITRO DIAGNOSTIC REAGENTS |
| BS ISO 17593:2007 | Clinical laboratory testing and in vitro medical devices. Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy |
| ISO 15198:2004 | Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturer |
| CLSI POCT4 A2 : 2ED 2006 | POINT-OF-CARE IN VITRO DIAGNOSTIC (IVD) TESTING |
| ISO 17593:2007 | Clinical laboratory testing and in vitro medical devices Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy |
| CLSI EP27 P : 1ED 2009 | HOW TO CONSTRUCT AND INTERPRET AN ERROR GRID FOR DIAGNOSTIC ASSAYS |
| CLSI POCT7 P : 1ED 2009 | QUALITY MANAGEMENT: APPROACHES TO REDUCING ERRORS AT THE POINT OF CARE |
| BS ISO 15198:2004 | Clinical laboratory medicine. In vitro diagnostic medical devices. Validation of user quality control procedures by the manufacturer |
| UNI CEN ISO/TS 22367 : 2010 | MEDICAL LABORATORIES - REDUCTION OF ERROR THROUGH RISK MANAGEMENT AND CONTINUAL IMPROVEMENT |
| DD ISO/TS 22367 : 2008 | MEDICAL LABORATORIES - REDUCTION OF ERROR THROUGH RISK MANAGEMENT AND CONTINUAL IMPROVEMENT |
| CLSI POCT13 A2 : 2ED 2005 | GLUCOSE MONITORING IN SETTINGS WITHOUT LABORATORY SUPPORT |
| S.R. CEN ISO TS 22367:2010 | MEDICAL LABORATORIES - REDUCTION OF ERROR THROUGH RISK MANAGEMENT AND CONTINUAL IMPROVEMENT |
| ISO/TS 22367:2008 | Medical laboratories Reduction of error through risk management and continual improvement |
| CEN ISO/TS 22367:2010 | Medical laboratories - Reduction of error through risk management and continual improvement (ISO/TS 22367:2008, including Cor 1:2009) |
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