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EN ISO 15194:2009

Current

Current

The latest, up-to-date edition.

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 15194:2009)

Published date

05-01-2009

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Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Systematic format of properties in the supporting
  documentation of a certified reference material
  4.1 Format of properties
  4.2 Construction of systematic designations
  4.3 Trivial names
5 Properties, production, and characterization of a
  certified reference material
  5.1 Hierarchical position
  5.2 Properties
  5.3 Production and characterization
6 Content of supporting documentation
  6.1 Supporting documentation
  6.2 Label
  6.3 Certificate
  6.4 Certification report
Annex A (informative) - Certified reference materials
        with nominal properties or ordinal quantities
Bibliography
Annex ZA (informative) - Relationship between this
         International Standard and the Essential
         Requirements of EU Directive 98/79

ISO 15194:2009 specifies requirements for certified reference materials and the content of their supporting documentation, in order for them to be considered of higher metrological order in accordance with ISO 17511. It is applicable to certified reference materials classifiable as primary measurement standards, secondary measurement standards and international conventional calibrators that function either as calibrators or trueness control materials. ISO 15194:2009 also provides requirements on how to collect data for value determination and how to present the assigned value and its measurement uncertainty.ISO 15194:2009 applies to certified reference materials with assigned values of differential or rational quantities. Annex A provides information on nominal properties and ordinal quantities.ISO 15194:2009 does not apply to reference materials that are parts of an in vitro diagnostic measuring system, although it is possible that many elements are helpful.

Committee
CEN/TC 140
DevelopmentNote
Supersedes EN 12287. (09/2009)
DocumentType
Standard
PublisherName
Comite Europeen de Normalisation
Status
Current

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ISO/IEC 17025:2005 General requirements for the competence of testing and calibration laboratories
ISO Guide 32:1997 Calibration in analytical chemistry and use of certified reference materials
ISO 15195:2003 Laboratory medicine Requirements for reference measurement laboratories
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ISO Guide 33:2015 Reference materials — Good practice in using reference materials
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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/IEC Guide 63:2012 Guide to the development and inclusion of safety aspects in International Standards for medical devices
ISO/IEC Guide 99:2007 International vocabulary of metrology Basic and general concepts and associated terms (VIM)
ISO/IEC Guide 15:1977 ISO/IEC code of principles on "reference to standards"
ISO/IEC Guide 51:2014 Safety aspects — Guidelines for their inclusion in standards
ISO 17511:2003 In vitro diagnostic medical devices Measurement of quantities in biological samples Metrological traceability of values assigned to calibrators and control materials
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ISO 5725-2:1994 Accuracy (trueness and precision) of measurement methods and results Part 2: Basic method for the determination of repeatability and reproducibility of a standard measurement method
ISO 14971:2007 Medical devices Application of risk management to medical devices
ISO Guide 31:2015 Reference materials — Contents of certificates, labels and accompanying documentation
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ISO Guide 34:2009 General requirements for the competence of reference material producers
ISO/IEC Guide 98-3:2008 Uncertainty of measurement — Part 3: Guide to the expression of uncertainty in measurement (GUM:1995)

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