Dosage Forms, Formulation Developments and Regulations
eBook - ePub

Dosage Forms, Formulation Developments and Regulations

Recent and Future Trends in Pharmaceutics, Volume 1

  1. 575 pages
  2. English
  3. ePUB (mobile friendly)
  4. Available on iOS & Android
eBook - ePub

Dosage Forms, Formulation Developments and Regulations

Recent and Future Trends in Pharmaceutics, Volume 1

About this book

Dosage Forms, Formulation Developments and Regulations, Volume One in the Recent and Future Trends in Pharmaceutics series, explores aspects of pharmaceutics, with an original approach focused on technology, novelties and future trends in the field. The book discusses the most recent developments in pharmaceutical preformulation and formulation studies, biopharmaceutics and novel pharmaceutical formulations, regulatory affairs, and good manufacturing practices. Exciting areas such as formulation strategies, optimization techniques, the biopharmaceutical classification system, and pharmaceutical aerosols are included. The field of pharmaceutics is highly dynamic and rapidly expanding day-by-day, so it demands a variety of amplified efforts for designing and developing pharmaceutical processes and formulation strategies. This is an essential reference for researchers in academia and industry as well as advanced graduate students in pharmaceutics. - Examines trends and recent technologies in dosage, formulation and regulation - Contains contributions from leading experts in academia, research, industry and regulatory agencies - Includes high-quality illustrations, flow charts and tables for easy understanding of concepts - Discusses practical examples and research case studies

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Yes, you can access Dosage Forms, Formulation Developments and Regulations by Amit Kumar Nayak,Kalyan Kumar Sen in PDF and/or ePUB format, as well as other popular books in Medicine & Pharmaceutical, Biotechnology & Healthcare Industry. We have over one million books available in our catalogue for you to explore.

Table of contents

  1. Cover
  2. Title page
  3. Table of Contents
  4. Copyright
  5. Contents
  6. List of contributors
  7. About the editors
  8. Preface
  9. Acknowledgments
  10. List of Illustrations
  11. List of Tables
  12. Chapter 1 : New drug discovery and development
  13. Chapter 2 : Introduction to different types of dosage forms and commonly used excipients
  14. Chapter 3 : Pharmacopoeias, national formulary and extra pharmacopoeia
  15. Chapter 4 : Regulatory affairs: historical overview, authorities, and role in drug approval
  16. Chapter 5 : Introduction to intellectual property rights and drug patents
  17. Chapter 6 : Introduction to pharmaceutical validation
  18. Chapter 7 : Design of dosage forms: influences of anatomy and administration routes
  19. Chapter 8 : Formulation strategies to improve the bioavailability of poorly absorbed drugs
  20. Chapter 9 : Optimization techniques in pharmaceutical formulation and processing
  21. Chapter 10 : Pharmaceutical product development: a “quality by design” (QbD) approach
  22. Chapter 11 : Pharmaceutical excipients
  23. Chapter 12 : Pharmaceutical calculations
  24. Chapter 13 : Preformulation considerations in pharmaceutical formulation process
  25. Chapter 14 : Biopharmaceutical Classification System: a strategic tool in pharmaceutical formulation
  26. Chapter 15 : Technology development and transfer in pharmaceutical product development
  27. Chapter 16 : Recent developments in pharmaceutical liquids
  28. Chapter 17 : Advances in semisolid dosage form
  29. Chapter 18 : Pharmaceutical sterilization
  30. Chapter 19 : Pharmaceutical sterile formulations
  31. Chapter 20 : Dermatological formulations
  32. Chapter 21 : Pharmaceutical aerosols
  33. Chapter 22 : Pharmaceutical packaging: recent trends and challenges
  34. Index
  35. A