CLSI EP17 A2 : 2ED 2012
Current
The latest, up-to-date edition.
EVALUATION OF DETECTION CAPABILITY FOR CLINICAL LABORATORY MEASUREMENT PROCEDURES
Hardcopy , PDF
English
18-06-2012
Abstract
Committee Membership
Foreword
1 Scope
2 Standard Precautions
3 Terminology
4 Background
5 Protocols for Evaluation of the Limit of Blank
and Limit of Detection
6 Protocol for Evaluation of the Limit of Quantitation
7 Verification of Detection Capability Claims
8 Reporting Detection Capability
References
Appendix A - Worked Example: Evaluation of Limits
of Blank and Detection by the Classical
Approach
Appendix B - Worked Example: Evaluation of Limit
of Detection by the Precision Profile Approach
Appendix C - Worked Example: Evaluation of Limit
of Detection by the Probit Approach
Appendix D - Worked Examples: Evaluation of Limit
of Quantitation
Appendix E - Worked Example: Verification of Limits
of Blank and Detection Claims
Appendix F - Worked Example: Verification of Limit
of Quantitation Claim
The Quality Management System Approach
Related CLSI Reference Materials
Gives guidance for evaluation and documentation of the detection capability of clinical laboratory measurement procedures (ie, limits of blank, detection, and quantitation), for verification of manufacturers' detection capability claims, and for the proper use and interpretation of different detection capability estimates.
DevelopmentNote |
Supersedes CLSI EP17 A. (07/2012)
|
DocumentType |
Miscellaneous Product
|
ISBN |
1-56238-796-0
|
Pages |
80
|
PublisherName |
Clinical Laboratory Standards Institute
|
Status |
Current
|
Supersedes |
CLSI MM23 : 1ED 2015 | MOLECULAR DIAGNOSTIC METHODS FOR SOLID TUMORS (NONHEMATOLOGICAL NEOPLASMS) |
CLSI EP19 : 2ED 2015 | A FRAMEWORK FOR USING CLSI DOCUMENTS TO EVALUATE CLINICAL LABORATORY MEASUREMENT PROCEDURES |
CLSI MM7 A2 : 2ED 2013 | FLUORESCENCE IN SITU HYBRIDIZATION METHODS FOR CLINICAL LABORATORIES |
CLSI H48 : 2ED 2016 | DETERMINATION OF COAGULATION FACTOR ACTIVITIES USING THE ONE-STAGE CLOTTING ASSAY |
CLSI EP34:2018(R2023) | Establishing and Verifying an Extended Measuring Interval Through Specimen Dilution and Spiking |
CLSI C49:2018(R2023) | Analysis of Body Fluids in Clinical Chemistry |
CLSI NBS06 A : 1ED 2013 | NEWBORN BLOOD SPOT SCREENING FOR SEVERE COMBINED IMMUNODEFICIENCY BY MEASUREMENT OF T-CELL RECEPTOR EXCISION CIRCLES |
CLSI POCT17 : 1ED 2016 | USE OF GLUCOSE METERS FOR CRITICALLY ILL PATIENTS |
CLSI NBS07 : 1ED 2017 | NEWBORN BLOOD SPOT SCREENING FOR POMPE DISEASE BY LYSOSOMAL ACID A-GLUCOSIDASE ACTIVITY ASSAYS |
PD ISO/TS 17822-1:2014 | <i>In</i> <i>vitro</i> diagnostic test systems. Qualitative nucleic acid-based <i>in</i> <i>vitro</i> examination procedures for detection and identification of microbial pathogens General requirements, terms and definitions |
CLSI I/LA20 : 3ED 2016 | ANALYTICAL PERFORMANCE CHARACTERISTICS, QUALITY ASSURANCE, AND CLINICAL UTILITY OF IMMUNOLOGICAL ASSAYS FOR HUMAN IMMUNOGLOBULIN E ANTIBODIES OF DEFINED ALLERGEN SPECIFICITIES |
CLSI C57 : 1ED 2015 | MASS SPECTROMETRY FOR ANDROGEN AND ESTROGEN MEASUREMENTS IN SERUM |
CLSI MM22 A : 1ED 2014 | MICROARRAYS FOR DIAGNOSIS AND MONITORING OF INFECTIOUS DISEASES |
CLSI EP36 : 1EDE 2015 | HARMONIZATION OF SYMBOLOGY AND EQUATIONS |
CLSI MM3 A3 : 3ED 2015 | MOLECULAR DIAGNOSTIC METHODS FOR INFECTIOUS DISEASES |
CLSI EP15 A3 : 3ED 2014 | USER VERIFICATION OF PRECISION AND ESTIMATION OF BIAS |
CLSI EP5 A3 : 3ED 2014 | Evaluation of Precision of Quantitative Measurement Procedures; Approved Guideline—Third Edition<br> |
CLSI C40 A2 : 2ED 2013 | MEASUREMENT PROCEDURES FOR THE DETERMINATION OF LEAD CONCENTRATIONS IN BLOOD AND URINE |
CLSI EP9 A3 : 3ED 2013 | MEASUREMENT PROCEDURE COMPARISON AND BIAS ESTIMATION USING PATIENT SAMPLES |
ISO/TS 17822-1:2014 | In vitro diagnostic test systems Qualitative nucleic acid-based in vitro examination procedures for detection and identification of microbial pathogens Part 1: General requirements, terms and definitions |
CLSI EP14 A2 : 2ED 2005 | EVALUATION OF MATRIX EFFECTS |
CLSI EP5 A2 : 2ED 2004 | EVALUATION OF PRECISION PERFORMANCE OF QUANTITATIVE MEASUREMENT METHODS |
CLSI EP12 A2 : 2ED 2008 | USER PROTOCOL FOR EVALUATION OF QUALITATIVE TEST PERFORMANCE |
CLSI EP6 A : 1ED 2003 | EVALUATION OF THE LINEARITY OF QUANTITATIVE MEASUREMENT PROCEDURES - A STATISTICAL APPROACH |
CLSI M29 A3 : 3ED 2005 | ACQUIRED INFECTIONS; APPROVED GUIDELINE |
CLSI EP29 A : 1ED 2012 | EXPRESSION OF MEASUREMENT UNCERTAINTY IN LABORATORY MEDICINE |
CLSI EP15 A2 : 2ED 2006 | USER VERIFICATION OF PERFORMANCE FOR PRECISION AND TRUENESS |
CLSI EP7 A2 : 2ED 2005 | INTERFERENCE TESTING IN CLINICAL CHEMISTRY |
CLSI MM3 A2 : 2ED 2006 | MOLECULAR DIAGNOSTIC METHODS FOR INFECTIOUS DISEASES |
Access your standards online with a subscription
Features
-
Simple online access to standards, technical information and regulations.
-
Critical updates of standards and customisable alerts and notifications.
-
Multi-user online standards collection: secure, flexible and cost effective.