CLSI EP34:2018(R2023)
Current
The latest, up-to-date edition.
Establishing and Verifying an Extended Measuring Interval Through Specimen Dilution and Spiking
Hardcopy , PDF
English
03-01-2023
This guideline provides procedures for establishing, validating, and verifying a dilution scheme to use for obtaining results for patient specimens with measurand concentrations or activity values above a measurement procedure’s upper limit of quantitation (ULoQ).
DocumentType |
Standard
|
ISBN |
978-1-68440-014-0
|
Pages |
94
|
PublisherName |
Clinical Laboratory Standards Institute
|
Status |
Current
|
Supersedes |
ISO 5725-1:2023 | Accuracy (trueness and precision) of measurement methods and results — Part 1: General principles and definitions |
ISO 15193:2009 | In vitro diagnostic medical devices Measurement of quantities in samples of biological origin Requirements for content and presentation of reference measurement procedures |
CLSI EP17 A2 : 2ED 2012 | EVALUATION OF DETECTION CAPABILITY FOR CLINICAL LABORATORY MEASUREMENT PROCEDURES |
ISO 18153:2003 | In vitro diagnostic medical devices — Measurement of quantities in biological samples — Metrological traceability of values for catalytic concentration of enzymes assigned calibrators and control materials |
ISO 17511:2020 | In vitro diagnostic medical devices Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples |
ISO 15195:2018 | Laboratory medicine — Requirements for the competence of calibration laboratories using reference measurement procedures |
ISO 18113-1:2022 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements |
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