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Pharmaceuticals bioequivalence

WA Ritschel, DD Denson. Influence of disease on bioavailability. In PG Welling, FLS Tse, SV Dighe, eds. Pharmaceutical Bioequivalence. New York Marcel Dekker, 1991, pp. 67-115. [Pg.75]

Pharmaceutical Bioequivalence, edited by Peter G. Welling, Francis L. S. Tse, and Shrikant V. Dinghe... [Pg.6]

Dressman JB and Yamada K (1991) Animal Models for Oral Absorption. In PG Welling, FLS Tse, SV Dinghe (Eds.), Pharmaceutical Bioequivalence, VI48. New York, Dekker, pp 727-739. [Pg.75]

Dressman JB, Yamada K. 1991. Animal models for oral drug absorption. In Pharmaceutical Bioequivalence, ed. P Welling, FL Welling, pp. 235-66. New York Dekker... [Pg.170]

Dighe SV, Adams WP. Bioequivalence A United States regulatory perspective. In Welling PG, Tse FLS, Dighe SV, eds. Pharmaceutical Bioequivalence, 1st edn. New York Marcel Dekker, 1991 347 80. [Pg.127]

Reprinted from Animal models for oral drug absorption, by J. B. Dressman and K. Yamada in Pharmaceutical Bioequivalence, ... [Pg.278]

Preclinical Dmg Disposition A Laboratory Handbook, Francis L. S. Tse and James J. Jaffe 47. HPLC in the Pharmaceutical Industry, edited by Godwin W Fong and Stanley K. Lam 48. Pharmaceutical Bioequivalence, edited by Peter G. Welling, Francis L. S. Tse, andShrikant V. Dinghe... [Pg.920]


See other pages where Pharmaceuticals bioequivalence is mentioned: [Pg.760]    [Pg.545]    [Pg.337]    [Pg.633]    [Pg.474]    [Pg.651]    [Pg.431]    [Pg.175]    [Pg.290]    [Pg.659]    [Pg.387]    [Pg.619]   
See also in sourсe #XX -- [ Pg.256 ]




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Bioequivalency

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