1. Goodman and Gilman’s: The Pharmacological Basis of Therapeutics, New York: McGraw-Hill, 1996, 9th ed.
2. Metodicheskie ukazaniya. Provedenie kachestvennykh issledovanii bioekvivalentnosti lekarstvennykh sredstv (Methodological Regulations: Qualitative Study of the Bioequivalence of Pharmaceutical Preparations), Moscow: Minzdrav RF, 2004.
3. In vivo Bioequivalence Guidances, United States Pharmacopeia 30 and National Formulary 25 (USP 30 NF 25), 2007.
4. Guidance for Industry: Bioanalytical Method Validation, US Department of Health and Human Services, Food and Drug Administration Centre for Drug Evaluation and Research (CDER), Centre for Veternary Medicine (CVM), 2001, http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM070107.pdf .
5. Clarke’s Analysis of Drugs and Poisons, Moffat, A.C., Osselton, M.D., and Widdop, B., Eds., London: Pharmaceutical Press, 2004.