This book volume provides complete and updated information on the applications of Design of Experiments (DoE) and related multivariate techniques at various stages of pharmaceutical product development. It discusses the applications of experimental designs that shall include oral, topical, transdermal, injectables preparations, and beyond for nanopharmaceutical product development, leading to dedicated case studies on various pharmaceutical experiments through illustrations, art-works, tables and figures. 

This book is a valuable guide for all academic and industrial researchers, pharmaceutical and biomedical scientists, undergraduate and postgraduate research scholars, pharmacists, biostatisticians, biotechnologists, formulations and process engineers, regulatory affairs and quality assurance personnel. 

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This book volume provides complete and updated information on the applications of Design of Experiments (DoE) and related multivariate techniques at various stages of pharmaceutical product development.

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Chapter 1. Introduction to the application of experimental designs in pharmaceutical product development.- Chapter 2. Design of experiments for the development of solid oral dosage forms.- Chapter 3. Design of experiments for the development of topical drug products.- Chapter 4. Design of experiments for the development of transdermal drug products.- Chapter 5. Design of experiments for the development of injectable drug products.- Chapter 6. Design of experiments for the development of inhalational products.- Chapter 7. Design of experiments for the development of ophthalmic products.- Chapter 8. Design of experiments for the development of vesicular drug products.- Chapter 9. Design of experiments for the development of nanoparticles, nanomaterials, and nanocomposites.- 

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This book volume provides complete and updated information on the applications of Design of Experiments (DoE) and related multivariate techniques at various stages of pharmaceutical product development. It discusses the applications of experimental designs that shall include oral, topical, transdermal, injectables preparations, and beyond for nanopharmaceutical product development, leading to dedicated case studies on various pharmaceutical experiments through illustrations, art-works, tables and figures. 

This book is a valuable guide for all academic and industrial researchers, pharmaceutical and biomedical scientists, undergraduate and postgraduate research scholars, pharmacists, biostatisticians, biotechnologists, formulations and process engineers, regulatory affairs and quality assurance personnel. 
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Explains the concept of Design of Experiment (DoE) and its applications Talks about the various types and applications of experimental designs Presents dedicated pharmaceutical product development case studies
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GPSR Compliance The European Union's (EU) General Product Safety Regulation (GPSR) is a set of rules that requires consumer products to be safe and our obligations to ensure this. If you have any concerns about our products you can contact us on ProductSafety@springernature.com. In case Publisher is established outside the EU, the EU authorized representative is: Springer Nature Customer Service Center GmbH Europaplatz 3 69115 Heidelberg, Germany ProductSafety@springernature.com
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Produktdetaljer

ISBN
9789813343504
Publisert
2021-01-23
Utgiver
Vendor
Springer Verlag, Singapore
Høyde
235 mm
Bredde
155 mm
Aldersnivå
Research, P, 06
Språk
Product language
Engelsk
Format
Product format
Innbundet

Redaktør

Om bidragsyterne

Dr. Sarwar Beg is currently serving as Assistant Professor of Pharmaceutics & Biopharmaceutics at School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi, Dr Sarwar has expertise in implementation of Quality by Design (QbD) in formulation development and analytical development of generic products. He has over a decade of experience in systematic development and characterization of novel and nanostructured drug delivery systems using QbD paradigms including Design of Experiments (DoE), Quality Risk Management (QRM), Multivariate Chemometric Approaches, Advanced Biopharmaceutics and Pharmacokinetic. Besides, Dr Sarwar has acquired know-how of applying advanced release kinetic modeling, pharmacokinetic modeling and in vitro/in vivo correlation (IVIVC) for efficient development of drug products. Till date, he has authored over 170 publications including research and review papers in high impact peer-reviewed journals, 10 journal special issues, 13 books, 45 book chapters and 3 Indian patent applications. He currently serves as the Regional Editor-Asia of the journal Current Nanomedicine (Bentham Science) and is an editorial board member of several other journals. He has been awarded with prestigious “Sun Pharma Science Foundation Award 2017” by Hon’ble Health Minister of India, “Innovative Pharma Researcher Award 2016” by SIPRA Lab (Hyderabad), “Eudragit® Award 2014” in South-Asia by M/s Evonik (Germany), “Budding QbD Scientist Award 2014” and “Budding ADME Scientist Award 2013” by M/s Select Biosciences (UK) and “Novartis Biocamp Award 2012” (Hyderabad). Besides, Dr Sarwar is a visiting researcher to many academic institutes/universities and pharma industrial houses for delivering expert lectures and hands-on training seminars.