Bioequivalence and Bioavailability Forum

Good point, DLabes.
First: "In studies to determine bioequivalence after a single dose, AUC_t, AUC_oo, C_max and t_max should be determined."
And then later:
"The assessment of bioequivalence is based upon 90% confidence intervals for the ratio of the population geometric means (test/reference) for the parameters under consideration."
One could get the impression that the pharmacokinetolophystic subgroup is requesting a parametric analysis of t_max including 90% CI's and the works, had it not been for the final punch:
"In studies to determine bioequivalence after a single dose, the parameters to be analysed are AUC_t and C_max."
...so why do they want t_max at all?

EM.