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How to Develop Robust Solid Oral Dosage Forms
From Conception to Post-Approval
As part of the Expertise in Pharmaceutical Process Technology Series, this book uses a hands-on approach to cover the development process of solid oral dosage forms
Bhavishya Mittal (Author)
9780128047316, Elsevier Science
Paperback, published 5 October 2016
190 pages
22.9 x 15.1 x 1.3 cm, 0.32 kg
"Readers will get a good overview of each topic, alongside practical advice and illustrative case studies. Decision trees and reference tables are particularly useful. ... This excellent book provides a great introduction for anyone starting a career in formulation science, and is a perfect starting point for trouble shooting issues throughout the formulation development process." --Emma McConnell, The Pharmaceutical Journal
How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval uses a practical and hands-on approach to cover the development process of solid oral dosage forms in one single source. The book details all of the necessary steps from formulation through the post-approval phase and contains industry case studies, real world advice, and troubleshooting tips. By merging the latest scientific information with practical instructions, this book provides pharmaceutical scientists in formulation research and development with a concrete look at the key aspects in the development of solid oral dosage forms.
1. Rules of Drug Product Development2. Pharmacokinetics and Preformulation3. Formulation Development4. Pharmaceutical Unit Operations5. Process Development6. Analytical Considerations7. Process Scale-up, Tech-Transfer, and Optimization8. Business Acuity
Subject Areas: Pharmacology [MMG], Pharmaceutical industries [KNDP]
