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Diagnostické zdravotnické prostředky in vitro - Požadavky na stanovení metrologické návaznosti hodnot přiřazených kalibrátorům, kontrolním materiálům pravdivosti a humánním vzorkům (Norma k přímému použití jako ČSN).
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NORMA vydána dne 1.12.2021
Označení normy: ČSN EN ISO 17511-ed.2
Třídící znak: 857020
Katalogové číslo: 513191
Datum vydání normy: 1.12.2021
Kód zboží: NS-1043013
Počet stran: 72
Přibližná hmotnost: 216 g (0.48 liber)
Země: Česká technická norma
Kategorie: Technické normy ČSN
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-commercial organizations producing RMs for use by many end-users of IVD MDs and/or calibration laboratories, or for use by a single end-user medical laboratory, as in the case of a measurement standard (calibrator) intended to be used exclusively for calibration of a laboratory-developed MP.
This document is applicable to:
This document is not applicable to:
NOTE 2 - Nominal scales are typically used to report e.g. identity of blood cell types, microorganism types, identity of nucleic acid sequences, identity of urine particles.
NOTE 3 - Ordinal scales are often applied to results differentiated into dichotomous groupings (e.g. ´sick´ vs. ´healthy´), and occasionally to results differentiated into non-dichotomous categories where the result categories are rank-ordered but the rank-ordered categories cannot be differentiated in terms of relative degree of difference, e.g. negative, +1, +2, +3 for grading of presence of haemoglobin in urine specimens by visual observation
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