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Titlebook: Biopharmaceutics Applications in Drug Development; Rajesh Krishna,Lawrence Yu Book 2008 Springer-Verlag US 2008 absorption.bioequivalence.

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发表于 2025-3-21 18:14:34 | 显示全部楼层 |阅读模式
期刊全称Biopharmaceutics Applications in Drug Development
影响因子2023Rajesh Krishna,Lawrence Yu
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发行地址discusses state of the art knowledge in biopharmaceutics.identifies key issues and opportunities in a distinct problem-solving approach
图书封面Titlebook: Biopharmaceutics Applications in Drug Development;  Rajesh Krishna,Lawrence Yu Book 2008 Springer-Verlag US 2008 absorption.bioequivalence.
影响因子.Drug performance is a vital aspect of new drug development as it draws on interdisciplinary expertise from both pharmaceutics and pharmacokinetics disciplines. It is at the key interface that the discipline of biopharmaceutics has emerged. The past two decades have witnessed considerable advances in biopharmaceutics, particularly with regard to bioavailability/bioequivalence, product quality and regulatory standards of approval...Biopharmaceutics Applications in Drug Development presents readers with step-wise, detail-conscious information to develop quality pharmaceuticals. It is composed of carefully crafted sections introducing key concepts and advances in the areas of dissolution, BA/BE, BCS, IVIC, and product quality, with specific focus on integration of regulatory considerations and case histories highlighting the biopharmaceutics strategies adopted in development of successful drugs. .
Pindex Book 2008
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Bioavailability and Bioequivalence,lay a significant role in the discovery, development, and regulation of new drug products. Additionally, bioequivalence studies are a crucial component of abbreviated new drug applications (ANDAs), leading to market access of safe, effective, and low cost generic drugs.
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fully crafted sections introducing key concepts and advances in the areas of dissolution, BA/BE, BCS, IVIC, and product quality, with specific focus on integration of regulatory considerations and case histories highlighting the biopharmaceutics strategies adopted in development of successful drugs. .978-1-4419-4434-4978-0-387-72379-2
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Christian Werner,Volker Klein,Konradin Webervailability assessment, highlight issues regarding their utilities and limitations, and review challenges of improving some of these current dissolution methods, particularly those used for assessing . drug product performance. In this chapter, we first provide some background information on dissolu
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R. Bombach,B. Hemmerling,W. Kreutnerlay a significant role in the discovery, development, and regulation of new drug products. Additionally, bioequivalence studies are a crucial component of abbreviated new drug applications (ANDAs), leading to market access of safe, effective, and low cost generic drugs.
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