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1 ion capabilities (<2%), acceptable accuracy (intra-assay 92-113%, inter-assay 69-138%) and precision
13 rassay CVs < 3% and ICCs > 99%; urine assay, intra-assay CV = 7.7% and ICC = 98.2% and interassay CV
14 s 12 pg/mL and 20 pg/mL respectively with an intra-assay CV of 11.3% at the CCbeta and an average rec
15 sing conventional chromogenic IHC and showed intra-assay heterogeneity (E1L3N coefficient of variatio
16 a less than 15% coefficient of variation for intra-assay, interassay, and interoperator variability.
19 assay demonstrated high levels of inter- and intra-assay precision and accuracy, and the linear range
20 h specificity to detect ApoB-100, acceptable intra-assay precision and good stability, functioning as
23 tration levels for each analyte demonstrated intra-assay precision of < or =2.5% coefficient of varia
27 performed on spiked specimens for linearity, intra-assay precision, interassay precision, limit of de
32 nt samples were used to determine inter- and intra-assay reproducibility and linearity, which were ve
33 , S/N = 3), high specificity, good inter-and intra-assay reproducibility and satisfactory storage sta
36 To achieve this goal, the QAP required an intra-assay standard deviation of no greater than 0.15 l
37 monstrated highly reproducible results, with intra-assay standard deviations (measured in log(10) RNA
42 rrelation coefficient, > or = 0.88) and good intra-assay variability in laboratory 3 (correlation coe
44 iations including interassay variability and intra-assay variability of the assays were modest, i.e.,
46 he PC biosensor assay in terms of inter- and intra-assay variability, spike-recovery (%), limit of de
49 alidation parameters such as inter-assay and intra-assay variation gave values of <5% coefficient of
50 e: the coefficient of variance of inter- and intra-assay variation is between 3.9% and 9.8% for all a
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