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How to Develop Robust Solid Oral Dosage Forms from Conception to PostApproval uses a practical and handson 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 postapproval 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. Focuses on important topics, such as robustness, bioavailability, formulation design, continuous processing, stability tests, modified release dosage forms, international guidelines, process scaleup, and much more Part of the Expertise in Pharmaceutical Process Technology series edited by Michael Levin Discusses common, realworld problems and offers both theoretical and practical solutions to these everyday issues
⚠️ WARNING (California Proposition 65):
This product may contain chemicals known to the State of California to cause cancer,
birth defects, or other reproductive harm.
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