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Introduction to Quality by Design (QbD)from theory to practice /

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Introduction to Quality by Design (QbD)edited by N. K. Jain, Neha Bajwa.
其他題名:	from theory to practice /
其他作者:	Jain, N. K.
出版者:	Singapore :Springer Nature Singapore :2024.
面頁冊數:	xxiv, 493 p. :ill., digital ;24 cm.
Contained By:	Springer Nature eBook
標題:	DrugsDesign.
電子資源:	https://doi.org/10.1007/978-981-99-8034-5
ISBN:	9789819980345$q(electronic bk.)

Introduction to Quality by Design (QbD)from theory to practice /
Introduction to Quality by Design (QbD)from theory to practice /[electronic resource] :edited by N. K. Jain, Neha Bajwa. - Singapore :Springer Nature Singapore :2024. - xxiv, 493 p. :ill., digital ;24 cm.

Chapter 1. Introduction to Quality by Design -- Chapter 2. Regulatory Aspects of Quality by Design (USFDA, PMDA, ICH, EMEA guidelines) -- Chapter 3. Criteria for selection of Design (PAT, CMA,CPA,CQA,RMEA) -- Chapter 4. Analytical Quality by Design -- Chapter 5. API Quality by Design -- Chapter 6. Quality by Design for formulation development -- Chapter 7. Quality by Design for oral formulations (tablets, spheroids) -- Chapter 8. Quality by Design for topical formulations -- Chapter 9. Quality by Design for parenteral formulations -- Chapter 10. Quality by Design approach for Novel Drug Delivery Systems -- Chapter 11. Quality by Design for herbal products/ formulations -- Chapter 12. Quality by Design in Quality Assurance -- Chapter 13. Quality by Design in pharmaceutical packaging -- Chapter 14. Quality by Design and Clinical Trials -- Chapter 15. Applications of Quality by design -- Chapter 16. Quality by Design and Marketing -- Chapter 17. Conclusions and Future perspective.

This book offers a comprehensive exploration of the Quality by Design (QbD) methodology, guiding readers from theory to practical application with accessible examples. It equips readers with both foundational and advanced knowledge, emphasizing the critical parameters necessary for designing pharmaceutical products that meet the highest quality standards. The book goes beyond theory to demonstrate how to effectively implement QbD principles in various aspects of pharmaceutical research and development, including analytical methods, formulation, and packaging processes. Through a step-by-step approach, it prepares researchers in pharmaceutical sciences, as well as professionals in the pharmaceutical and healthcare industries (including suppliers), to successfully integrate QbD into their work.

ISBN: 9789819980345$q(electronic bk.)

Standard No.: 10.1007/978-981-99-8034-5doiSubjects--Topical Terms:

201742
Drugs
--Design.

LC Class. No.: RS189

Dewey Class. No.: 615.19

Introduction to Quality by Design (QbD)from theory to practice /
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505 0 $a Chapter 1. Introduction to Quality by Design -- Chapter 2. Regulatory Aspects of Quality by Design (USFDA, PMDA, ICH, EMEA guidelines) -- Chapter 3. Criteria for selection of Design (PAT, CMA,CPA,CQA,RMEA) -- Chapter 4. Analytical Quality by Design -- Chapter 5. API Quality by Design -- Chapter 6. Quality by Design for formulation development -- Chapter 7. Quality by Design for oral formulations (tablets, spheroids) -- Chapter 8. Quality by Design for topical formulations -- Chapter 9. Quality by Design for parenteral formulations -- Chapter 10. Quality by Design approach for Novel Drug Delivery Systems -- Chapter 11. Quality by Design for herbal products/ formulations -- Chapter 12. Quality by Design in Quality Assurance -- Chapter 13. Quality by Design in pharmaceutical packaging -- Chapter 14. Quality by Design and Clinical Trials -- Chapter 15. Applications of Quality by design -- Chapter 16. Quality by Design and Marketing -- Chapter 17. Conclusions and Future perspective.
520 $a This book offers a comprehensive exploration of the Quality by Design (QbD) methodology, guiding readers from theory to practical application with accessible examples. It equips readers with both foundational and advanced knowledge, emphasizing the critical parameters necessary for designing pharmaceutical products that meet the highest quality standards. The book goes beyond theory to demonstrate how to effectively implement QbD principles in various aspects of pharmaceutical research and development, including analytical methods, formulation, and packaging processes. Through a step-by-step approach, it prepares researchers in pharmaceutical sciences, as well as professionals in the pharmaceutical and healthcare industries (including suppliers), to successfully integrate QbD into their work.
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