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封面: |
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题名: |
How to Develop Robust Solid Oral Dosage Forms: From Conception to Post-Approval |
作者: |
Bhavishya Mittal |
出版社: |
Elsevier Inc. |
出版日期: |
2016-10-05 |
ISBN: |
978-0-12-804731-6 |
附属页: |
齐全 |
书签: |
有 |
格式: |
清晰PDF |
内容简介: |
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
Key Features
Focuses on important topics, such as robustness, bioavailability, formulation design, continuous processing, stability tests, modified release dosage forms, international guidelines, process scale-up, and much more
Part of the Expertise in Pharmaceutical Process Technology series edited by Michael Levin
Discusses common, real-world problems and offers both theoretical and practical solutions to these everyday issues
Description
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.
Readership
Pharmaceutical scientists in formulation and research and development, academic professors and graduate students in pharmaceutical sciences and pharmacology |
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