Bioequivalence and bioequivalency testing

American Journal of Pharmaceutical Education

Volumn 63, Issue 2, 1999, Pages 194-198

  Balthasar, Joseph P ^a  

^a UNIVERSITY OF UTAH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0001161124     PISSN: 00029459     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (13)

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9. Shah, V.P., Yacobi, A., Barr, W.H., Benet, L.Z., Breimer, D., Dobrinska, M.R., Endrenyi, L., Fairweather, W., Gillespie, W, Gonzalez, M.A., Hooper, J., Jackson, A., Lesko, L.J., Midha, K.K., Noonan, P.K., Patnaik, R. and Williams, R.L., "Evaluation of orally administered highly variable drugs and drug formulations," Pharm Res, 13, 1590-1594(1996).
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13. Food and Drug Administration - Center for Drug Evaluation and Research, In vivo bioequivalence studies based on population and individual bioequivalence approaches - Draft guidance [may be accessed from: http://www.fda.gov/cder/guidance/index.htm], (1997).