Statistical Methods For Pharmaceutical Research Planning
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Statistical Methods For Pharmaceutical Research Planning
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Author : S. W. Bergman
language : en
Publisher: CRC Press
Release Date : 2020-10-29
Statistical Methods For Pharmaceutical Research Planning written by S. W. Bergman and has been published by CRC Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2020-10-29 with Mathematics categories.
This book focuses on statistical methods which impinge more or less directly on the decisions that are made during the course of pharmaceutical and agro-chemical research, considering the four decision-making areas.
Statistical Methodology In The Pharmaceutical Sciences
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Author : D. A. Berry
language : en
Publisher: CRC Press
Release Date : 2016-04-19
Statistical Methodology In The Pharmaceutical Sciences written by D. A. Berry and has been published by CRC Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2016-04-19 with Mathematics categories.
A state-of-the-art handbook of statistical analysis for use in the pharmaceutical industry. Areas covered in this reference/text include: bioavailability, repeated-measures designs, dose-response, population models, multicenter trials, handling dropouts, survival analysis, robust data analysis, cate
Applied Statistics In The Pharmaceutical Industry
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Author : Steven P. Millard
language : en
Publisher: Springer Science & Business Media
Release Date : 2013-11-09
Applied Statistics In The Pharmaceutical Industry written by Steven P. Millard and has been published by Springer Science & Business Media this book supported file pdf, txt, epub, kindle and other format this book has been release on 2013-11-09 with Medical categories.
Providing a general guide to statistical methods used in the pharmaceutical industry, and illustrating how to use S-PLUS to implement these methods, the book explains why S-PLUS is a useful software package and discusses the results and implications of each particular application. It is targeted at graduates in biostatistics, statisticians involved in the industry as research scientists, regulators, academics, and/or consultants who want to know more about how to use S-PLUS and learn about other sub-fields within the industry, as well as statisticians in other fields who want to know more about statistical applications in the pharmaceutical industry.
Planning Pharmaceutical Clinical Trials
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Author : William M. Wooding
language : en
Publisher: Wiley-Interscience
Release Date : 1994
Planning Pharmaceutical Clinical Trials written by William M. Wooding and has been published by Wiley-Interscience this book supported file pdf, txt, epub, kindle and other format this book has been release on 1994 with Mathematics categories.
Imparts a working understanding of the statistical principles and procedures essential to conducting successful clinical studies. Features a detailed catalog of experimental designs most commonly used in clinical work. Includes two chapters on elementary applied statistics and one on sample size estimation (the number of patients required).
Introduction To Statistics In Pharmaceutical Clinical Trials
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Author : Todd A. Durham
language : en
Publisher:
Release Date : 2008-01-01
Introduction To Statistics In Pharmaceutical Clinical Trials written by Todd A. Durham and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2008-01-01 with Mathematics categories.
All students of pharmaceutical sciences and clinical research need a solid knowledge and understanding of the nature, methods, application, and importance of statistics. Introduction to Statistics in Pharmaceutical Clinical Trials is an ideal introduction to statistics presented in the context of clinical trials conducted during pharmaceutical drug development. This novel approach both teaches the computational steps needed to conduct analyses and provides a conceptual understanding of how these analyses provide information that forms the rational basis for decision making throughout the drug development process.
Statistical Design And Analysis In Pharmaceutical Science
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Author : Shein-Chung Chow
language : en
Publisher: CRC Press
Release Date : 2018-10-03
Statistical Design And Analysis In Pharmaceutical Science written by Shein-Chung Chow and has been published by CRC Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2018-10-03 with Mathematics categories.
"Offers a comprehensive, unified presentation of statistical designs and methods of analysis for all stages of pharmaceutical development--emphasizing biopharmaceutical applications and demonstrating statistical techniques with real-world examples."
Statistical Methods For Pharmaceutical Research Planning
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Author : S. W. Bergman
language : en
Publisher: CRC Press
Release Date : 2020-10-28
Statistical Methods For Pharmaceutical Research Planning written by S. W. Bergman and has been published by CRC Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2020-10-28 with Mathematics categories.
This book focuses on statistical methods which impinge more or less directly on the decisions that are made during the course of pharmaceutical and agro-chemical research, considering the four decision-making areas.
Hybrid Frequentist Bayesian Power And Bayesian Power In Planning Clinical Trials
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Author : Andrew P. Grieve
language : en
Publisher: CRC Press
Release Date : 2022-06-19
Hybrid Frequentist Bayesian Power And Bayesian Power In Planning Clinical Trials written by Andrew P. Grieve and has been published by CRC Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2022-06-19 with Mathematics categories.
Hybrid Frequentist/Bayesian Power and Bayesian Power in Planning Clinical Trials provides a practical introduction to unconditional approaches to planning randomised clinical trials, particularly aimed at drug development in the pharmaceutical industry. This book is aimed at providing guidance to practitioners in using average power, assurance and related concepts. This book brings together recent research and sets them in a consistent framework and provides a fresh insight into how such methods can be used. Features: A focus on normal theory linking average power, expected power, predictive power, assurance, conditional Bayesian power and Bayesian power. Extensions of the concepts to binomial, and time-to-event outcomes and non-inferiority trials An investigation into the upper bound on average power, assurance and Bayesian power based on the prior probability of a positive treatment effect Application of assurance to a series of trials in a development program and an introduction of the assurance of an individual trial conditional on the positive outcome of an earlier trial in the program, or to the successful outcome of an interim analysis Prior distribution of power and sample size Extension of the basic approach to proof-of-concept trials with dual success criteria Investigation of the connection between conditional and predictive power at an interim analysis and power and assurance Introduction of the idea of surety in sample sizing of clinical trials based on the width of the confidence intervals for the treatment effect, and an unconditional version.
Innovative Strategies Statistical Solutions And Simulations For Modern Clinical Trials
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Author : Mark Chang
language : en
Publisher: CRC Press
Release Date : 2019-03-20
Innovative Strategies Statistical Solutions And Simulations For Modern Clinical Trials written by Mark Chang and has been published by CRC Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2019-03-20 with Mathematics categories.
"This is truly an outstanding book. [It] brings together all of the latest research in clinical trials methodology and how it can be applied to drug development.... Chang et al provide applications to industry-supported trials. This will allow statisticians in the industry community to take these methods seriously." Jay Herson, Johns Hopkins University The pharmaceutical industry's approach to drug discovery and development has rapidly transformed in the last decade from the more traditional Research and Development (R & D) approach to a more innovative approach in which strategies are employed to compress and optimize the clinical development plan and associated timelines. However, these strategies are generally being considered on an individual trial basis and not as part of a fully integrated overall development program. Such optimization at the trial level is somewhat near-sighted and does not ensure cost, time, or development efficiency of the overall program. This book seeks to address this imbalance by establishing a statistical framework for overall/global clinical development optimization and providing tactics and techniques to support such optimization, including clinical trial simulations. Provides a statistical framework for achieve global optimization in each phase of the drug development process. Describes specific techniques to support optimization including adaptive designs, precision medicine, survival-endpoints, dose finding and multiple testing. Gives practical approaches to handling missing data in clinical trials using SAS. Looks at key controversial issues from both a clinical and statistical perspective. Presents a generous number of case studies from multiple therapeutic areas that help motivate and illustrate the statistical methods introduced in the book. Puts great emphasis on software implementation of the statistical methods with multiple examples of software code (both SAS and R). It is important for statisticians to possess a deep knowledge of the drug development process beyond statistical considerations. For these reasons, this book incorporates both statistical and "clinical/medical" perspectives.
Research Methods For Pharmaceutical Practice And Policy
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Author : Rajender R. Aparasu
language : en
Publisher: Pharmaceutical Press
Release Date : 2011
Research Methods For Pharmaceutical Practice And Policy written by Rajender R. Aparasu and has been published by Pharmaceutical Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2011 with Medical categories.
This text provides the theory and practice for conducting pharmaceutical policy research. It covers all aspects of scientific research from conceptualising to statistical analysis. It also provides scientific basis and a good understanding of the principles and practice of conducting pharmaceutical policy research.