Pharmaceutical quality by design principles and applications / edited by Sarwar Beg, MD Saquib Hasnain.
| Other author | Beg, Sarwar, 1987- |
| Other author | Hasnain, Md Saquib, 1984- |
| Format | Electronic |
| Publication Info | London, United Kingdom ; San Diego, CA, United States : Elsevier/Academic Press, [2019] |
| Description | xxi, 426 pages : illustrations (some color) ; 23 cm |
| Supplemental Content | Full text available from eBook - Pharmacology, Toxicology and Pharmaceutical Science 2019 |
| Subjects |
| Uniform title | Pharmaceutical quality by design (Beg) |
| Contents | 1. Introduction to Quality by Design (QbD): Fundamentals, principles -- 2. Global regulatory perspectives on Quality by Design in pharma manufacturing -- 3. Application of Design of Experiments (DoE) in pharmaceutical product and process optimization -- 4. QbD considerations for excipient manufacturing -- 5. QbD considerations for analytical development -- 6. Application of Quality by Design paradigms for development of solid dosage forms -- 7. QbD considerations for topical and transdermal product development -- 8. Qbd based development of pharmaceutical parenteral drug products: An overview -- 9. Quality by design considerations for product development of dry-powder inhalers -- 10. QbD considerations for development of lyophilized products -- 11. Application of quality by design approach for hot-melt extrusion process optimization -- 12. QbD applications for development of nanopharmaceutical products -- 13. Application of QbD principles in nanocarrier based drug delivery systems -- 14. Application of QbD framework for development of self-emulsifying drug delivery systems -- 15. 'Quality by Design' approach for development of multiparticulate drug delivery systems -- 16. Application of QbD elements for development of vesicular drug delivery systems -- 17. Emergence of quality by design in extraction technology for bioactive compounds -- 18. Application of quality by design for the development of biopharmaceuticals. |
| Abstract | Pharmaceutical Quality by Design: Principles and Applications discusses the Quality by Design (QbD) concept implemented by regulatory agencies to ensure the development of a consistent and high-quality pharmaceutical product that safely provides the maximum therapeutic benefit to patients. The book walks readers through the QbD framework by covering the fundamental principles of QbD, the current regulatory requirements, and the applications of QbD at various stages of pharmaceutical product development, including drug substance and excipient development, analytical development, formulation development, dissolution testing, manufacturing, stability studies, bioequivalence testing, risk and assessment, and clinical trials. Contributions from global leaders in QbD provide specific insight in its application in a diversity of pharmaceutical products, including nanopharmaceuticals, biopharmaceuticals, and vaccines. The inclusion of illustrations, practical examples, and case studies makes this book a useful reference guide to pharmaceutical scientists and researchers who are engaged in the formulation of various delivery systems and the analysis of pharmaceutical product development and drug manufacturing process. |
| Bibliography note | Includes bibliographical references and index. |
| Access restriction | Available only to authorized users. |
| Technical details | Mode of access: World Wide Web |
| Genre/form | Electronic books. |
| LCCN | 2019938744 |
| ISBN | 9780128157992 paperback |
| ISBN | 0128157992 paperback |
Availability
| Library | Location | Call Number | Status | Item Actions |
|---|---|---|---|---|
| Electronic Resources | Access Content Online | ✔ Available |