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DSF/PREN ISO 15194

In vitro diagnostic medical devices – Requirements for certified reference materials and the content of supporting documentation (ISO/DIS 15194:2023)

pending
Organization: DS
Status: pending
Page Count: 31
ICS Code (In vitro diagnostic test systems): 11.100.10
scope:

This standard specifies requirements for producers of CRMs of higher metrological order and the content of their supporting documentation that comply with the requirements of ISO 17511 and the calibration hierarchies described therein. It is applicable to CRMs intended for use as either primary reference materials, secondary calibrators or international conventional calibrators within calibration hierarchies appropriate for measurands used in laboratory medicine, or for applications as trueness controls. Requirements for determining the certified value of a CRM, including evaluation and reporting of the assigned uncertainty, are specified. This standard applies primarily to CRMs with assigned property values where the property has a magnitude that can be expressed as a quantitative scalar number or ratio to a reference or refers to a counting scale as also described in the scope of ISO 17511:2020. Annex A provides information on CRMs for qualitative nominal properties and ordinal quantities, to provide guidance on important quality attributes for such CRMs, whilst recognizing that they are not within the metrological traceability schemes described in ISO 17511:2020. When a CRM includes multiple measurands, this Standard is applied to each of the certified quantity values present in the CRM. Although intended to be applicable to producers of CRMs, this Standard will also be useful for RMs that do not comply with the full metrological requirements of CRMs. For example, this International Standard does not apply to a RM created by IVD MD manufacturers for use as working calibrator or end-user calibrator within a calibration hierarchy traceable to a CRM, although some content may be useful in assessing its performance.

Document History

June 11, 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
This International Standard specifies requirements for certified reference materials and the content of their supporting documentation for them to be considered as higher order according to ISO...
DSF/PREN ISO 15194
In vitro diagnostic medical devices – Requirements for certified reference materials and the content of supporting documentation (ISO/DIS 15194:2023)
This standard specifies requirements for producers of CRMs of higher metrological order and the content of their supporting documentation that comply with the requirements of ISO 17511 and the...
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/DIS 15194:2007)
This European Standard specifies requirements and formats for the description of reference materials. It is applicable to reference materials of higher metrological order, classifiable as primary...
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/FDIS 15194:2009)
This International Standard specifies requirements for certified reference materials and the content of their supporting documentation, in order for them to be considered of higher metrological order...
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