Design and Analysis of Bioavailability and Bioequivalence Studies

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A01=Jen-pei Liu
A01=Shein-Chung Chow
advanced bioequivalence study design
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ation
Author_Jen-pei Liu
Author_Shein-Chung Chow
average
Average Bioavailabilities
Average Bioequivalence
balanced incomplete block design
bioavailabilities
bioavailability
bioequivalence
Bioequivalence Limit
Bioequivalence Studies
Carryover Effects
Category=PS
clinical trial methodology
crossover design
Direct Drug Effect
Direct Formulation Effect
drug
drug formulation analysis
Drug Product
eq_bestseller
eq_isMigrated=1
eq_isMigrated=2
eq_nobargain
eq_non-fiction
eq_science
esis
Ft FR
Generic Drug Product
Higher Order Crossover Design
hypoth
Individual Bioequivalence
Innovator Drug Product
Intra-subject Variabilities
Intrasubject Variability
log-linear model
meta-analysis
pharmaceutical statistics
Pharmacokinetic Responses
pharmacokinetics
pharmacometric modeling
Population Bioequivalence
product
refere
Reference Formulation
Reference Products
regulatory compliance
samp
sample size determination
Shein-Chung Chow
T1 T2
therapeutic equivalence
Unequal Carryover Effects
varia
weighted least squares method
YT Yr

Product details

  • ISBN 9781584886686
  • Weight: 1224g
  • Dimensions: 156 x 234mm
  • Publication Date: 15 Oct 2008
  • Publisher: Taylor & Francis Inc
  • Publication City/Country: US
  • Product Form: Hardback
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Preeminent Experts Update a Well-Respected Book

Taking into account the regulatory and scientific developments that have occurred since the second edition, Design and Analysis of Bioavailability and Bioequivalence Studies, Third Edition provides a complete presentation of the latest progress of activities and results in bioavailability and bioequivalence on regulatory requirements, scientific and practical issues, and statistical methodology.

New to the Third Edition

  • Four new chapters that present a thorough account of novel developments in the field
  • New and updated sections that reflect recent advances in the statistical methodology in the design and analysis of bioavailability and bioequivalence studies
  • Reorganization of the material into five parts, making it easier to access related information together
  • Over 100 new references from the literature

Like its bestselling predecessors, this edition covers all of the statistical problems that may occur in the various stages of design and data analysis. Keeping the mathematics and statistics at a fundamental level, it continues to focus on practical concepts rather than technical details.

Duke University School of Medicine, Durham, North Carolina, National Taiwan University, Taipei, Taiwan

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