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Pharmaceutical bioequivalence / edited by Peter G. Welling, Francis L.S. Tse, and Shrikant V. Dighe

Contributor(s): Welling, Peter G [editor] | Tse, Francis L.S [editor] | Dighe, Shrikant V [editor]Material type: Text

TextPublication details: New York : Dekker, c1991Description: ix, 467 pages : illustrations ; 23 cmISBN: 0824784847Subject(s): DRUGS -- THERAPEUTIC EQUIVALENCY | DRUG EVALUATION | DRUGS -- ADMINISTRATION & DOSAGELOC classification: RM 301.45 .P43 1991

Contents:

Part one: Bioequivalence and Its Determination -- Part two: Species differences, pharmacodynamic models -- Part three: Perspectives of regulatory agencies, worldwide, on bioequivalence testing

Summary: Is essential reading for pharmacists adn pharmacologists, drug regulatroy personnel, and upper-level undergraduate and graduate students in these disciplines.

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Item type	Current library	Home library	Collection	Shelving location	Call number	Copy number	Status	Date due	Barcode
Books	LRC - Main	National University - Manila	Pharmacy	General Circulation	GC RM 301.45 .P43 1991 (Browse shelf (Opens below))	c.1	Available		NULIB000003910

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Previous	GC RM 301.28 .R63 2004 Introductory clinical pharmacology /	GC RM 301.28 .T64 2005 The hands-on guide to clinical pharmacology /	GC RM 301.28 .T69 2008 Case files : Eugene C. Toy [and three others].	GC RM 301.45 .P43 1991 Pharmaceutical bioequivalence /	GC RM 302.4 .D78 1973 vol.226 Drug-protein binding /	GC RM 302.5 .T49 1991 Textbook of adverse drug reactions /	GC RM 302.5 .U54 2011 Understanding pharmacoepidemiology /	Next

Includes bibliographic references and index.

Part one: Bioequivalence and Its Determination -- Part two: Species differences, pharmacodynamic models -- Part three: Perspectives of regulatory agencies, worldwide, on bioequivalence testing

Is essential reading for pharmacists adn pharmacologists, drug regulatroy personnel, and upper-level undergraduate and graduate students in these disciplines.

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