Generic Drug Product Development
eBook - PDF

Generic Drug Product Development

International Regulatory Requirements for Bioequivalence

  1. 334 pages
  2. English
  3. PDF
  4. Available on iOS & Android
eBook - PDF

Generic Drug Product Development

International Regulatory Requirements for Bioequivalence

About this book

Due to a worldwide need for lower cost drug therapy, use of generic and multi-source drug products have been increasing. To meet international patent and trade agreements, the development and sale of these products must conform to national and international laws, and generic products must prove that they are of the same quality and are therapeutica

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Information

Publisher
CRC Press
Year
2016
Print ISBN
9781841847849
eBook ISBN
9781420020021
Edition
1
Topic
Medicine
Subtopic
Pharmacology

Table of contents

  1. Front Cover
  2. Preface
  3. Acknowledgements
  4. Disclaimer
  5. Annexure 1
  6. Contents
  7. Contributors
  8. Chapter 1. Introduction
  9. Chapter 2. Australasia
  10. Chapter 3. Brazil
  11. Chapter 4. Canada
  12. Chapter 5. The European Union
  13. Chapter 6. India
  14. Chapter 7. Japan
  15. Chapter 8. South Africa
  16. Chapter 9. South America and Pan American Health Organization
  17. Chapter 10. Taiwan
  18. Chapter 11. Turkey
  19. Chapter 12. United States of America
  20. Chapter 13. The World Health Organization
  21. Index
  22. Back Cover

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Yes, you can access Generic Drug Product Development by Isadore Kanfer, Leon Shargel, Isadore Kanfer,Isadore Kanfer,Leon Shargel,Leon Shargel, Isadore Kanfer, Isadore Kanfer, Leon Shargel, Leon Shargel in PDF and/or ePUB format, as well as other popular books in Medicine & Pharmacology. We have over 1.5 million books available in our catalogue for you to explore.