Handbook of Pharmaceutical Wet Granulation, 9780443298172
Hardcover
Master wet granulation: theory, practice, and quality in a design paradigm.
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Handbook of Pharmaceutical Wet Granulation

theory and practice in a quality by design paradigm

$569.83

  • Hardcover

    900 pages

  • Release Date

    1 November 2025

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Summary

The Wet Granulation Handbook: A Practical Guide to Pharmaceutical Manufacturing

Handbook of Pharmaceutical Wet Granulation: Theory and Practice in a Quality by Design Paradigm, Second Edition offers a single and comprehensive reference dedicated to all aspects of pharmaceutical wet granulation, taking a holistic approach by combining introductory principles with practical solutions.

Chapters are written by international experts across industry, academic and regulatory settin…

Book Details

ISBN-13:9780443298172
ISBN-10:0443298173
Author:Ajit S. Narang, Sherif I.F. Badawy
Publisher:Elsevier Science Publishing Co Inc
Imprint:Academic Press Inc
Format:Hardcover
Number of Pages:900
Edition:2nd
Release Date:1 November 2025
Weight:450g
Dimensions:279mm x 216mm
About The Author

Ajit S. Narang

Ajit S. Narang works for the Bristol-Myers Squibb, Co. in New Brunswick, New Jersey, in the biopharmaceutical aspects of drug delivery. He has more than eight years of experience in the pharmaceutical industry in the development of oral dosage forms and drug delivery platforms. In addition to the Bristol-Myers Squibb, Co., he has worked for Ranbaxy Research Labs in Gurgaon, India, and Morton Grove Pharmaceuticals in Vernon Hills, Illinois. He has more than 35 publications and three pending patent applications and has contributed to the development of several marketed drug products.

Sherif Badawy, Ph.D., is a Research Fellow in the Drug product Science and Technology of the Bristol-Myers Squibb Company. He received his B.S. in Pharmacy and M.S. in Pharmaceutics from Cairo University, and his Ph.D. in Pharmaceutics from Duquesne University. He has more than 20 years of industrial experience in drug product development. His current responsibilities at Bristol-Myers Squibb include formulation and process development and scale-up of commercial oral solid and liquid dosage forms. His areas of research interest include high shear wet granulation, tablet compaction, stability of solid dosage forms and bioavailability enhancement of poorly water-soluble compounds. He authored more than 40 manuscripts and numerous abstracts and presentations in those areas.

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