Clinical Trials Handbook PDF ePub eBook

Books Info:

Clinical Trials Handbook free pdf Best practices for conducting effective and safe clinical trials Clinical trials are arguably the most important steps in proving drug effectiveness and safety for public use. They require intensive planning and organization and involve a wide range of disciplines: data management, biostatistics, pharmacology, toxicology, modeling and simulation, regulatory monitoring, ethics, and particular issues for given disease areas. Clinical Trials Handbook provides a comprehensive and thorough reference on the basics and practices of clinical trials. With contributions from a range of international authors, the book takes the reader through each trial phase, technique, and issue. Chapters cover every key aspect of preparing and conducting clinical trials, including: Interdisciplinary topics that have to be coordinated for a successful clinical trialData management (and adverse event reporting systems) Biostatistics, pharmacology, and toxicology Modeling and simulation Regulatory monitoring and ethics Particular issues for given disease areas-cardiology, oncology, cognitive, dementia, dermatology, neuroscience, and more With unique information on such current issues as adverse event reporting (AER) systems, adaptive trial designs, and crossover trial designs, Clinical Trials Handbook will be a ready reference for pharmaceutical scientists, statisticians, researchers, and the many other professionals involved in drug development.

About Shayne C. Gad

Shayne Cox Gad, PhD, DABT, ATS , is the Principal of Gad Consulting Services. Dr. Gad has more than thirty years of experience as a toxicologist, statistical consultant, manager, and general consultant on research and development in the chemical, consumer product, contract testing, biotechnology, medical device, and pharmaceutical industries. He is the author of thirty-nine books and numerous papers, presentations, and other publications.

Details Book

Author : Shayne C. Gad
Publisher : Wiley-Blackwell (an imprint of John Wiley
Data Published : 29 May 2008
ISBN : 0471213888
EAN : 9780471213888
Format Book : PDF, Epub, DOCx, TXT
Number of Pages : 1248 pages
Age + : 15 years
Language : English
Rating :

Reviews Clinical Trials Handbook



17 Comments Add a comment




Related eBooks Download


  • Randomised Response-Adaptive Designs in Clinical Trials free pdfRandomised Response-Adaptive Designs in Clinical Trials

    Randomised Response-Adaptive Designs in Clinical Trials presents methods for the randomised allocation of treatments to patients in sequential clinical trials. Emphasizing the practical application of clinical trial designs..


  • Clinical Trials in Oncology free pdfClinical Trials in Oncology

    Studies that are unimpeachably thorough. non-political. unbiased. and properly designed. These are the standards to which everyone in clinical research aspires. Yet. the difficulties in designing trials and interpreting data are subtle and ever present..


  • Design and Analysis of Clinical Trials free pdfDesign and Analysis of Clinical Trials

    Praise for the Second Edition: "...a grand feast for biostatisticians. It stands ready to satisfy the appetite of any pharmaceutical scientist with a respectable statistical appetite." --Journal of Clinical Research Best Practices The Third Edition of Design and Analysis of Clinical Trials provides complete..


  • Introduction to Statistical Methods for Clinical Trials free pdfIntroduction to Statistical Methods for Clinical Trials

    Clinical trials have become essential research tools for evaluating the benefits and risks of new interventions for the treatment and prevention of diseases. from cardiovascular disease to cancer to AIDS..


  • The Use of Restricted Significance Tests in Clinical Trials free pdfThe Use of Restricted Significance Tests in Clinical Trials

    The reader will soon find that this is more than a "how-to-do-it" book. It describes a philosophical approach to the use of statistics in the analysis of clinical trials. I have come gradually to the position described here..


  • Clinical Trials Handbook free pdfClinical Trials Handbook

    . Best practices for conducting effective and safe clinical trials Clinical trials are arguably the most important steps in proving drug effectiveness and safety for public use. They require intensiv