CLSI C49:2018(R2023)
Current
Current
The latest, up-to-date edition.
Analysis of Body Fluids in Clinical Chemistry
Available format(s)
Hardcopy , PDF
Language(s)
English
Published date
23-08-2023
Publisher
C49 provides guidance to medical laboratories for the appropriate application of measurement procedures for body fluid testing and for reporting results.
DocumentType |
Standard
|
ISBN |
978-1-68440-023-2
|
Pages |
96
|
PublisherName |
Clinical Laboratory Standards Institute
|
Status |
Current
|
Supersedes |
ISO 15194:2009 | In vitro diagnostic medical devices Measurement of quantities in samples of biological origin Requirements for certified reference materials and the content of supporting documentation |
ISO 18113-1:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements |
CLSI EP17 A2 : 2ED 2012 | EVALUATION OF DETECTION CAPABILITY FOR CLINICAL LABORATORY MEASUREMENT PROCEDURES |
ISO 15189:2012 | Medical laboratories — Requirements for quality and competence |
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 9000:2015 | Quality management systems — Fundamentals and vocabulary |
CLSI EP19 : 2ED 2015 | A FRAMEWORK FOR USING CLSI DOCUMENTS TO EVALUATE CLINICAL LABORATORY MEASUREMENT PROCEDURES |
CLSI GP41 : 7ED 2017 | COLLECTION OF DIAGNOSTIC VENOUS BLOOD SPECIMENS |
CLSI EP10 A3 : 2006 + A1 2014 | PRELIMINARY EVALUATION OF QUANTITATIVE CLINICAL LABORATORY MEASUREMENT PROCEDURES |
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