Inhaled Pharmaceutical Product Development Perspectives
eBook - ePub

Inhaled Pharmaceutical Product Development Perspectives

Challenges and Opportunities

  1. 110 pages
  2. English
  3. ePUB (mobile friendly)
  4. Available on iOS & Android
eBook - ePub

Inhaled Pharmaceutical Product Development Perspectives

Challenges and Opportunities

Book details
Table of contents
Citations

About This Book

Inhaled Pharmaceutical Product Development Perspectives: Challenges and Opportunities describes methods and procedures for consideration when developing inhaled pharmaceuticals, while commenting on product development strategies and their suitability to support regulatory submission. It bridges the gap between the aspirations of scientists invested in new technology development and the requirements that must be met for any new product.

The book brings together emerging analytical and inhalation technologies, providing perspectives that illuminate formulation and device design, development, regulatory compliance, and practice. Focusing on underlying scientific and technical principles known to be acceptable from the current regulatory perspective, this monograph will remain useful as a high-level guide to inhaled product development for the foreseeable future.

  • Discusses development strategies and best practices in the context of regulatory requirements
  • Written by a broadly qualified expert drawing on the knowledge and critical opinions of key individuals in the field
  • Includes a foreword by Charles G. Thiel

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Yes, you can access Inhaled Pharmaceutical Product Development Perspectives by Anthony J. Hickey in PDF and/or ePUB format, as well as other popular books in Physical Sciences & Analytic Chemistry. We have over one million books available in our catalogue for you to explore.

Information

Publisher
Elsevier
Year
2017
ISBN
9780128123362

Table of contents

  1. Cover image
  2. Title page
  3. Table of Contents
  4. Copyright
  5. Dedication
  6. Foreword
  7. Preface
  8. Acknowledgments
  9. Chapter 1. Introduction—Historical Perspective
  10. Chapter 2. Dosage Forms
  11. Chapter 3. Quality and Performance Tests
  12. Chapter 4. Preclinical and Clinical Considerations
  13. Chapter 5. Regulatory Strategy
  14. Chapter 6. General Conclusion
  15. Index