CLSI EP14 A2 : 2ED 2005

Superseded

Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

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EVALUATION OF MATRIX EFFECTS

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Superseded date: 15-08-2014

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Published date: 12-01-2013

Publisher: Clinical Laboratory Standards Institute

Table of Contents - (Show below) - (Hide below)

Abstract
Committee Membership
Foreword
1 Scope
2 Introduction
3 Standard Precautions
4 Definitions
5 Principle of Evaluation
6 Protocols
  6.1 Materials
  6.2 Procedure
  6.3 Data Analysis
  6.4 Possible Variations
References
Additional References
Appendix A. A Hierarchical Diagram of Factors Affecting
            Reported Results
Appendix B. Data Input Form
Appendix C. Examples of Completed Analyses
Summary of Consensus/Delegate Comments and Committee Responses
The Quality System Approach
Related CLSI/NCCLS Publications

Abstract - (Show below) - (Hide below)

Specifies guidance for evaluating the bias in analyte measurements that is due to the sample matrix (physiological or artificial) when two measurement procedures are compared.

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Development Note	Supersedes NCCLS EP14 A (01/2005)
Document Type	Miscellaneous Product
ISBN
Pages
Published
Publisher	Clinical Laboratory Standards Institute
Status	Superseded
Superseded By	CLSI EP14 A3 : 2014
Supersedes	CLSI EP14 A : 1ED 2001

Standards Referenced By This Book - (Show below) - (Hide below)

CLSI EP32 R : 1ED 2006	METROLOGICAL TRACEABILITY AND ITS IMPLEMENTATION
CLSI EP18 A2 : 2ED 2009	RISK MANAGEMENT TECHNIQUES TO IDENTIFY AND CONTROL LABORATORY ERROR SOURCES
CLSI EP25 A : 1ED 2009	EVALUATION OF STABILITY OF IN VITRO DIAGNOSTIC REAGENTS
CLSI EP18 P3 : 3ED 2009	RISK MANAGEMENT TECHNIQUES TO IDENTIFY AND CONTROL LABORATORY ERROR SOURCES
CLSI MM17 P : 1ED 2007	VERIFICATION AND VALIDATION OF MULTIPLEX NUCLEIC ACID ASSAYS
CLSI EP7 A2 : 2ED 2005	INTERFERENCE TESTING IN CLINICAL CHEMISTRY
CLSI EP27 P : 1ED 2009	HOW TO CONSTRUCT AND INTERPRET AN ERROR GRID FOR DIAGNOSTIC ASSAYS
CLSI C49 P : 1ED 2006	ANALYSIS OF BODY FLUIDS IN CLINICAL CHEMISTRY
CLSI EP17 A2 : 2ED 2012	EVALUATION OF DETECTION CAPABILITY FOR CLINICAL LABORATORY MEASUREMENT PROCEDURES
CLSI POCT9 P : 1ED 2009	SELECTION CRITERIA FOR POINT-OF-CARE TESTING DEVICES
CLSI I/LA32 P : 1ED 2009	NEWBORN SCREENING BY TANDEM MASS SPECTROMETRY
CLSI EP30 A : 1ED 2010	CHARACTERIZATION AND QUALIFICATION OF COMMUTABLE REFERENCE MATERIALS FOR LABORATORY MEDICINE
CLSI MM6 A2 : 2ED 2010	QUANTITATIVE MOLECULAR METHODS FOR INFECTIOUS DISEASES
PD ISO Guide 34:2009	General requirements for the competence of reference material producers
CLSI MM17 A : 1ED 2008	VERIFICATION AND VALIDATION OF MULTIPLEX NUCLEIC ACID ASSAYS
ISO Guide 34:2009	General requirements for the competence of reference material producers
CLSI QMS01 A4 : 4ED 2011	QUALITY MANAGEMENT SYSTEM: A MODEL FOR LABORATORY SERVICES
CLSI NBS05 A : 1ED 2011	NEWBORN SCREENING FOR CYSTIC FIBROSIS
CLSI I/LA33 A : 1ED 2009	VALIDATION OF AUTOMATED SYSTEMS FOR IMMUNOHEMATOLOGICAL TESTING BEFORE IMPLEMENTATION
CLSI NBS04 A : 1ED 2010	NEWBORN SCREENING BY TANDEM MASS SPECTROMETRY
CLSI C53 P : 1ED 2008	CHARACTERIZATION AND QUALIFICATION OF COMMUTABLE REFERENCE MATERIALS FOR LABORATORY MEDICINE
CLSI EP18 P2 : 2ED 2007	RISK MANAGEMENT TECHNIQUES TO IDENTIFY AND CONTROL LABORATORY ERROR SOURCES
CLSI C49 A : 1ED 2007	ANALYSIS OF BODY FLUIDS IN CLINICAL CHEMISTRY
CLSI EP9 A3 : 3ED 2013	MEASUREMENT PROCEDURE COMPARISON AND BIAS ESTIMATION USING PATIENT SAMPLES
CLSI EP22 P : 1ED 2010	PRESENTATION OF A MANUFACTURER'S RISK MITIGATION INFORMATION FOR USERS OF IN VITRO DIAGNOSTIC DEVICES
CLSI GP27 A2 : 2ED 2007	USING PROFICIENCY TESTING TO IMPROVE THE CLINICAL LABORATORY
CLSI I/LA33 P : 1ED 2009	VALIDATION OF AUTOMATED DEVICES FOR IMMUNOHEMATOLOGIC TESTING PRIOR TO IMPLEMENTATION
CLSI I/LA26 A2 : 2ED 2013	PERFORMANCE OF SINGLE CELL IMMUNE RESPONSE ASSAYS

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