ÍST EN ISO 17511:2003

Staða:

Fellur úr gildi - 15.7.2021

Íslenskt heiti:

Lækningatæki til sjúkdómsgreininga í glasi - Magnmæling í lífrænum sýnum - Mælifræðilegur rekjanleiki gilda sem tiltekin eru fyrir kvörðunartæki og samanburðarefni.

Enskt heiti:

In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values assigned to calibrators and control materials

Tengdur staðall:

ISO/FDIS 17511:2002

Tækninefnd:

CEN/TC 140

ICS flokkur:

7.100

Auglýst:

15.7.2021

Umfang (scope):

Lækningatæki til sjúkdómsgreininga í glasi - Magnmæling í lífrænum sýnum - Mælifræðilegur rekjanleiki gilda sem tiltekin eru fyrir kvörðunartæki og samanburðarefni.

Hafðu samband í síma 520-7150 varðandi þennan staðal.

Mynd sem fylgir ÍST EN ISO 17511:2021

ÍST EN ISO 17511:2021

This document specifies technical requirements and documentation necessary to establish metrological traceability of values assigned to calibrators, trueness control materials and human samples for quantities measured by IVD MDs. The human samples are those intended to be measured, as specified for each IVD MD. Metrological traceability of values for quantities in human samples extends to the highest available reference system component, ideally to RMPs and certified reference materials (CRMs). All parties having a role in any of the steps described in a calibration hierarchy for an IVD MD are subject to the requirements described. These parties include but are not limited to manufacturers (of IVD MDs), RMP developers (see ISO 15193), RM producers (see ISO 15194), and reference/calibration laboratories (see ISO 15195) supporting calibration hierarchies for IVD MDs. NOTE 1 Producers of RMs intended for use in standardization or calibration of IVD MDs include commercial and non-commerc
Verð: 16.544 kr.
Mynd sem fylgir ÍST EN ISO 17511:2021

ÍST EN ISO 17511:2021

This document specifies technical requirements and documentation necessary to establish metrological traceability of values assigned to calibrators, trueness control materials and human samples for quantities measured by IVD MDs. The human samples are those intended to be measured, as specified for each IVD MD. Metrological traceability of values for quantities in human samples extends to the highest available reference system component, ideally to RMPs and certified reference materials (CRMs). All parties having a role in any of the steps described in a calibration hierarchy for an IVD MD are subject to the requirements described. These parties include but are not limited to manufacturers (of IVD MDs), RMP developers (see ISO 15193), RM producers (see ISO 15194), and reference/calibration laboratories (see ISO 15195) supporting calibration hierarchies for IVD MDs. NOTE 1 Producers of RMs intended for use in standardization or calibration of IVD MDs include commercial and non-commerc
Verð: 16.544 kr.
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