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Generics and Bioequivalence , Jackson, Andre J., 1994 CRC Press Rare HB Book
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Entrega prevista entre el jue. 20 nov. y el lun. 24 nov. a 94104
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N.º de artículo de eBay:386739781743
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Características del artículo
- Estado
- Country of Origin
- United States
- Book Title
- Generics and Bioequivalence
- Educational Level
- Adult & Further Education
- Level
- Advanced, Technical
- ISBN
- 9780849369308
Acerca de este producto
Product Identifiers
Publisher
CRC Press LLC
ISBN-10
0849369304
ISBN-13
9780849369308
eBay Product ID (ePID)
492681
Product Key Features
Number of Pages
224 Pages
Language
English
Publication Name
Generics and Bioequivalence
Subject
Pharmacy, Pharmacology
Publication Year
1994
Type
Textbook
Subject Area
Medical
Format
Hardcover
Dimensions
Item Height
0.7 in
Item Weight
16.8 Oz
Item Length
9.5 in
Item Width
6.3 in
Additional Product Features
Intended Audience
Scholarly & Professional
LCCN
93-044588
Dewey Edition
20
Illustrated
Yes
Dewey Decimal
615/.1
Table Of Content
Statistical Methods in Bioequivalence (E. Ormsby). Role of Single- and Multiple-Dose Studies in the Estimation of Bioequivalency (A.J. Jackson). The Role of Metabolites in Bioequivalency Assessment (M.-L. Chen and A.J. Jackson). Analytical Aspects of Bioequivalency Testing (J. Leslie). Pharmacodynamics and Bioequivalence (N.H.G. Holford). In Vivo and In Vitro Correlations: Scientific and Regulatory Perspectives (V.P. Shah and R.L. Williams). Stereochemical Considerations in Bioavailability Studies (W.R. Ravis and J.S. Owen). Animal Models and Their Role in Bioequivalence Studies (W.J. Adams). Commentary I: Issues in Bioequivalence: An Industrial Scientist's Perspective (P.K. Narang). Commentary II: Progress in Harmonization of Bioavailability and Bioequivalence Standards (I.J. McGilveray).
Synopsis
Generics and Bioequivalence provides a clear, insightful, and in-depth analysis of the many complex issues encountered in the determination of drug bioequivalence. Included are timely updates on many controversial and newly emerging areas in the design and analysis of bioavailability and bioequivalence studies. This new reference was prepared by a group of authorities from academe, industry, and government and can be easily understood by students and experienced scientists alike. Topics presented include the role of single and multiple dosing in the determination of bioequivalence, the role of metabolites in assessing bioequivalence, stereochemical considerations in bioequivalence evaluation, uses of animal models, pharmacodynamics, and statistics. The analysis of pharmacodynamic data (especially when plasma levels are unavailable) is covered, and the nascent importance of individual bioequivalence is examined.
LC Classification Number
RM301.45.G46 1994
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