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  • How to Validate a Pharmaceutical Process

    Series series Expertise in Pharmaceutical Process Technology
    How to Validate a Pharmaceutical Process provides a "how to approach to developing and implementing a sustainable pharmaceutical process validation program. The latest volume in the Expertise in Pharmaceutical Process Technology Series, this book illustrates the methods and reasoning behind processes and protocols. It also addresses practical problems and offers solutions to qualify and validate a ... Read more

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  • Equipment Qualification in the Pharmaceutical Industry

    Series series Aspects of Pharmaceutical Manufacturing
    Equipment Qualification in the Pharmaceutical Industry provides guidance and basic information for the preparation of a quality qualification program. It has been noted that there is a general lack of understanding in the industry, especially for those new to the industry, as to what constitutes a compliant qualification program. Even experienced professionals have felt a lack of security in ... Read more

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    Series series Rapid Review
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  • Lange Q & A Pharmacy, Tenth Edition

    Series series LANGE Q&A
    The most effective and comprehensive pharmacy review for the NAPLEX®The ultimate pharmacy review covering every topic tested on the exam1,500+ NAPLEX-style Q&As deliver unmatched preparation for the examBuild confidence and test-taking skills with more than 1500 NAPLEX®-style questions and tried-and-proven tips for boosting exam performanceLearn from detailed explanations why answers are cor... ... Read more

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  • Willful Ignorance

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    Series series Mathematics and Statistics (R0)
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  • Nonclinical Statistics for Pharmaceutical and Biotechnology Industries

    Series series Mathematics and Statistics (R0)
    This book serves as a reference text for regulatory, industry and academic statisticians and also a handy manual for entry level Statisticians. Additionally it aims to stimulate academic interest in the field of Nonclinical Statistics and promote this as an important discipline in its own right. This text brings together for the first time in a single volume a comprehensive survey of methods ... Read more

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  • Drug Stability for Pharmaceutical Scientists

    Drug Stability for Pharmaceutical Scientists is a clear and easy-to-follow guide on drug degradation in pharmaceutical formulation. This book features valuable content on both aqueous and solid drug solutions, the stability of proteins and peptides, acid-base catalyzed and solvent catalyzed reactions, how drug formulation can influence drug stability, the influence of external factors on reaction ... Read more

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    Guides You on the Development and Implementation of B–R EvaluationsBenefit–Risk Assessment Methods in Medical Product Development: Bridging Qualitative and Quantitative Assessments provides general guidance and case studies to aid practitioners in selecting specific benefit–risk (B–R) frameworks and quantitative methods. Leading experts from industry, regulatory agencies, and academia present ... Read more

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    Series series Mathematics and Statistics (R0)
    This edited volume is a definitive text on adaptive clinical trial designs from creation and customization to utilization. As this book covers the full spectrum of topics involved in the adaptive designs arena, it will serve as a valuable reference for researchers working in industry, government and academia. The target audience is anyone involved in the planning and execution of clinical trials, ... Read more

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