1. Pharmacokinetic determinants in the design and evaluation of sustained-release dosage forms;Boxenbaum;Pharmac. Res.,1984
2. The pharmacological and toxicological significance of stereochemistry of drug disposition;Caldwell;Xenobiotica,1988
3. Bioequivalence: a United States regulatory perspective;Dighe,1991
4. Sample size determination for bioequivalence assessment by means of confidence intervals;Diletti;Int. J. clin. Pharamac. Ther. Toxic.,1992
5. Sample size determination: extended tables for the multiplicative model and bioequivalence ranges of 0.9 to 1.11 and 0.7 to 1.43;Diletti;Int. J. clin. Pharmac. Ther. Toxic.,1992