CLSI I/LA20 : 3ED 2016
Current
The latest, up-to-date edition.
ANALYTICAL PERFORMANCE CHARACTERISTICS, QUALITY ASSURANCE, AND CLINICAL UTILITY OF IMMUNOLOGICAL ASSAYS FOR HUMAN IMMUNOGLOBULIN E ANTIBODIES OF DEFINED ALLERGEN SPECIFICITIES
Hardcopy, PDF
10-24-2016
Abstract
Committee Membership
Foreword
Chapter I - Introduction
Chapter 2 - Diagnosis of Human Immunoglobulin
E-Mediated Allergic Disease
Chapter 3 - Human Immunoglobulin E Primer
Chapter 4 - Specimens
Chapter 5 - Immunochemical Methods
Chapter 6 - Qualification of Assay of Reagents
Chapter 7 - Calibration Systems for Assays of
Immunoglobulin E Antibodies
Chapter 8 - Assay Performance Evaluation
Chapter 9 - Quality Assurance
Chapter 10 - Recommendation for Laboratories,
Medical Professional, and Clinical Laboratory
Inspectors
Chapter 11 - Design and Validation of an Immunoglobulin
E Antibody Immunoassay for New Biotherapeutic
Drugs in the Absence of a Drug-Specific Immunoglobulin
E Antibody Positive Control
Chapter 12 - Conclusion
Chapter 13 - Supplemental Information
References
Appendix A - Linearity (Dilution Recovery/Parallelism
Analysis)
Appendix B - Qualification of Anthihuman Immunoglobulin
E Reagents by Direct Binding Dilutional Analysis
and Competitive Inhibition Immunoassay
Appendix C - Qualification of Allergen-Containing Reagents
Appendix D - Precision/Reproducibility Testing of Assays
of Immunoglobulin E Antibodies
Appendix E - Lower Limit of Quantitation for an Immunoglobulin
E Antibody Assay
The Quality Management System Approach
Related CLSI References Materials
Gives guidance for the design, analytical performance, standardization, quality assurance, and clinical application of laboratory assays used in the measurement of human immunoglobulin E antibodies of defined allergen specificity.
DevelopmentNote |
Supersedes CLSI I/LA20 A2. (10/2016)
|
DocumentType |
Miscellaneous Product
|
ISBN |
1-56238-948-3
|
Pages |
120
|
PublisherName |
Clinical Laboratory Standards Institute
|
Status |
Current
|
Supersedes |
CLSI EP17 A2 : 2ED 2012 | EVALUATION OF DETECTION CAPABILITY FOR CLINICAL LABORATORY MEASUREMENT PROCEDURES |
CLSI EP5 A3 : 3ED 2014 | Evaluation of Precision of Quantitative Measurement Procedures; Approved Guideline—Third Edition<br> |
CLSI EP12 A2 : 2ED 2008 | USER PROTOCOL FOR EVALUATION OF QUALITATIVE TEST PERFORMANCE |
CLSI EP9 A3 : 3ED 2013 | MEASUREMENT PROCEDURE COMPARISON AND BIAS ESTIMATION USING PATIENT SAMPLES |
CLSI EP6 A : 1ED 2003 | EVALUATION OF THE LINEARITY OF QUANTITATIVE MEASUREMENT PROCEDURES - A STATISTICAL APPROACH |
CLSI EP25 A : 1ED 2009 | EVALUATION OF STABILITY OF IN VITRO DIAGNOSTIC REAGENTS |
CLSI C24 A3 : 3ED 2006 | STATISTICAL QUALITY CONTROL FOR QUANTITATIVE MEASUREMENT PROCEDURES: PRINCIPLES AND DEFINITIONS |
CLSI EP7 A2 : 2ED 2005 | INTERFERENCE TESTING IN CLINICAL CHEMISTRY |
CLSI M29 A4 : 4ED 2014 | Protection of Laboratory Workers From Occupationally Acquired Infections<br> |
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