Praised by practitioners, students and instructors for its engaging approach to teaching a very complex subject, Demystifying Opioid Conversion Calculations: A Guide for Effective Dosing, has long been the go-to guide for learning how to calculate opioid conversions. Now in its …
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Emphasizing the role of good statistical practices (GSP) in drug research and formulation, this book outlines important statistics applications for each stage of pharmaceutical development to ensure the valid design, analysis, and assessment of drug products under investigation …
This text outlines the applications of statistics for each stage of pharmaceutical development. It ensures the valid design, analysis and assessment of drug products under investigation and discusses the testing of population/individual bioequivalence and in vitro bioequivalence.
Chow (Temple U.) and Shao (U. of Wisconsin-Madison) explain the application of statistics used during the various stages of pharmaceutical research and development to demonstrate quality, safety, and efficacy in research and development. Among the contexts they consider are assa…
Published in 1994: This text focuses on the determination of bioequivalence between formulations that are pharmaceutically equivalent and manufactured using acceptable chemistry, manufacturing and controls and in accordance with Good Manufacturing Practices.
Discusses the worldwide legislative and regulatory requirements for the registration of generic and multi-source drug products.
Maintaining a practical perspective, Bioequivalence and Statistics in Clinical Pharmacology, Second Edition explores statistics used in day-to-day clinical pharmacology work. The book is a starting point for those involved in such research and covers the methods needed to design…
