Provides statistical workflows used in the evaluation of in vitro
diagnostic reagents. Facilities include method comparison, commutability
assessment, Bland-Altman and receiver operating characteristic analysis,
qualitative agreement, C5 and C95 estimation, precision and
variance-component analysis, linearity, interference, dilution and
spiking studies, high-dose hook assessment, measurement uncertainty,
reference-material bias, reference intervals, stability studies,
quality-control charts, curve fitting, analytical sensitivity, outlier and
normality assessment, and sample-size calculations. For methodological
details, see Bland and Altman (1986)