Design and Analysis of Bioavailability and Bioequivalence Studies
eBook - ePub

Design and Analysis of Bioavailability and Bioequivalence Studies

  1. 760 pages
  2. English
  3. ePUB (mobile friendly)
  4. Available on iOS & Android
eBook - ePub

Design and Analysis of Bioavailability and Bioequivalence Studies

About this book

Preeminent Experts Update a Well-Respected BookTaking 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 bioequiva

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Yes, you can access Design and Analysis of Bioavailability and Bioequivalence Studies by Shein-Chung Chow,Jen-pei Liu in PDF and/or ePUB format, as well as other popular books in Mathematics & Biostatistics. We have over one million books available in our catalogue for you to explore.

Information

Publisher
CRC Press
Year
2008
eBook ISBN
9781040067475
Edition
3
Topic
Mathematics
Subtopic
Biostatistics
Index
Mathematics

Table of contents

  1. Cover Page
  2. Halftitle Page
  3. Chapman & Hall/CRC Biostatistics Series
  4. Chapman & Hall/CRC Biostatistics Series
  5. Title Page
  6. Copyright Page
  7. Contents
  8. Preface
  9. Part I Preliminaries
  10. Chapter 1 Introduction
  11. Chapter 2 Design of Bioavailability Studies
  12. Chapter 3 Statistical Inferences for Effects from a Standard 2×2 Crossover Design
  13. Part II Average Bioequivalence
  14. Chapter 4 Statistical Methods for Average Bioequivalence
  15. Chapter 5 Power and Sample Size Determination
  16. Chapter 6 Transformation and Analysis of Individual Subject Ratios
  17. Chapter 7 Assessment of Inter- and Intra-Subject Variabilities
  18. Chapter 8 Assumptions of Outlier Detection for Average Bioequivalence
  19. Chapter 9 Optimal Crossover Designs for Two Formulations for Average Bioequivalence
  20. Chapter 10 Assessment of Bioequivalence for More Than Two Formulations
  21. Part III Population and Individual Bioequivalence
  22. Chapter 11 Population and Individual Bioequivalence
  23. Chapter 12 Statistical Procedures for Assessment of Population and Individual Bioequivalence
  24. Part IV In Vitro and Alternative Evaluation of Bioequivalence
  25. Chapter 13 Assessment of Bioequivalence for Drugs with Negligible Plasma Levels
  26. Chapter 14 In Vitro Bioequivalence Testing
  27. Chapter 15 In Vitro Dissolution Profiles Comparison
  28. Part V Other Bioequivalence Studies
  29. Chapter 16 Meta-Analysis for Bioequivalence Review
  30. Chapter 17 Population Pharmacokinetics
  31. Chapter 18 Other Pharmacokinetic Studies
  32. Chapter 19 Review of Regulatory Guidances on Bioequivalence
  33. Chapter 20 Frequently Asked Questions and Future Challenges
  34. References
  35. Appendix A Statistical Tables
  36. Appendix B SAS Programs
  37. Index