CLSI C49:2018(R2023)
Current
Current
Analysis of Body Fluids in Clinical Chemistry
Available format(s)
Hardcopy , PDF
Language(s)
English
Published date
08-23-2023
Publisher
US$273.60
Excluding Tax where applicable
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 |
| CLSI EP07 3ED : 2018 | Interference Testing in Clinical Chemistry, 3rd Edition |
| 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 |
| CLSI QMS24 : 3ED 2016 | USING PROFICIENCY TESTING AND ALTERNATIVE ASSESSMENT TO IMPROVE MEDICAL LABORATORY QUALITY |
| CLSI EP05-A3:2014(R2019) | Evaluation of Precision of Quantitative Measurement Procedures; Approved Guideline—Third Edition |
| CLSI EP6 A : 1ED 2003 | EVALUATION OF THE LINEARITY OF QUANTITATIVE MEASUREMENT PROCEDURES - A STATISTICAL APPROACH |
| 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 |
| CLSI EP15 A3 : 3ED 2014 | USER VERIFICATION OF PRECISION AND ESTIMATION OF BIAS |
| 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 QMS05 A2 : 2ED 2012 | QUALITY MANAGEMENT SYSTEM: QUALIFYING, SELECTING, AND EVALUATING A REFERRAL LABORATORY |
| CLSI GP41 : 7ED 2017 | COLLECTION OF DIAGNOSTIC VENOUS BLOOD SPECIMENS |
| CLSI EP10 A3 : 2006 + A1 2014 | PRELIMINARY EVALUATION OF QUANTITATIVE CLINICAL LABORATORY MEASUREMENT PROCEDURES |
| CLSI H56 A : 1ED 2006 | BODY FLUID ANALYSIS FOR CELLULAR COMPOSITION |
Summarise
US$273.60
Excluding Tax where applicable