How to Develop Robust Solid Oral Dosage Forms: From Conception to Post-Approval - Mittal, Bhavishya (Staff Fellow, Office of Pharmaceutical Quality (OPQ), Center for Drug Evaluation and Research (CDER), US Food and Drug Administration (FDA), Silver Spring, MD, USA) - Books - Elsevier Science Publishing Co Inc - 9780128047316 - October 13, 2016
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Mittal, Bhavishya (Staff Fellow, Office of Pharmaceutical Quality (OPQ), Center for Drug Evaluation and Research (CDER), US Food and Drug Administration (FDA), Silver Spring, MD, USA)
How to Develop Robust Solid Oral Dosage Forms: From Conception to Post-Approval

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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.--

190 pages

Media Books     Paperback Book   (Book with soft cover and glued back)
Released October 13, 2016
ISBN13 9780128047316
Publishers Elsevier Science Publishing Co Inc
Pages 190
Dimensions 228 × 154 × 14 mm   ·   317 g

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