How to Develop Robust Solid Oral Dosage Forms
eBook - ePub

How to Develop Robust Solid Oral Dosage Forms

From Conception to Post-Approval

  1. 190 pages
  2. English
  3. ePUB (mobile friendly)
  4. Available on iOS & Android
eBook - ePub

How to Develop Robust Solid Oral Dosage Forms

From Conception to Post-Approval

Book details
Table of contents
Citations

About This Book

How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval uses a practical and hands-on approach to cover the development process of solid oral dosage forms in one single source. The book details all of the necessary steps from formulation through the post-approval phase and contains industry case studies, real world advice, and troubleshooting tips.

By merging the latest scientific information with practical instructions, this book provides pharmaceutical scientists in formulation research and development with a concrete look at the key aspects in the development of solid oral dosage forms.

  • Focuses on important topics, such as robustness, bioavailability, formulation design, continuous processing, stability tests, modified release dosage forms, international guidelines, process scale-up, and much more
  • Part of the Expertise in Pharmaceutical Process Technology series edited by Michael Levin
  • Discusses common, real-world problems and offers both theoretical and practical solutions to these everyday issues

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Yes, you can access How to Develop Robust Solid Oral Dosage Forms by Bhavishya Mittal in PDF and/or ePUB format, as well as other popular books in Medicina & Farmacologia. We have over one million books available in our catalogue for you to explore.

Information

Year
2016
ISBN
9780128047323

Table of contents

  1. Cover image
  2. Title page
  3. Table of Contents
  4. Copyright
  5. Author Biography
  6. Foreword
  7. Preface
  8. Acknowledgments
  9. About the Expertise in Pharmaceutical Process Technology Series
  10. List of Abbreviations and Acronyms
  11. Chapter 1. Rules of Drug Product Development
  12. Chapter 2. Pharmacokinetics and Preformulation
  13. Chapter 3. Formulation Development
  14. Chapter 4. Pharmaceutical Unit Operations
  15. Chapter 5. Process Development
  16. Chapter 6. Analytical Considerations
  17. Chapter 7. Process Scale-up, Tech-Transfer, and Optimization
  18. Chapter 8. Business Acuity
  19. Index