2×2 Crossover BE Analysis
Perform a regulatory-grade 2×2 crossover bioequivalence assessment. Paste pre-computed NCA parameters (Cmax, AUClast, AUCinf) per subject per period, configure sequence labels, then click Run Crossover BE Analysis. Results include mixed-effects ANOVA (Type III SS), LS means, 90% CI via TOST, within-subject CV, and sequence/period effect diagnostics.