Wiley Encyclopedia of Clinical Trials PDF Download
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Author: Lisa Marie Sullivan
Publisher: Wiley-Blackwell
ISBN:
Category : Medical
Languages : en
Pages : 674
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Book Description
Here you'll find more than 500 entries from the world's leading experts in the field on the basic concepts, methodologies, and applications in clinical trials. The range of topics includes: basic statistical concepts, design and analysis of clinical trials, ethics, regulatory issues, and methodologies for clinical data management and analysis
Author: Lisa Marie Sullivan
Publisher: Wiley-Blackwell
ISBN:
Category : Medical
Languages : en
Pages : 674
Get Book Here
Book Description
Here you'll find more than 500 entries from the world's leading experts in the field on the basic concepts, methodologies, and applications in clinical trials. The range of topics includes: basic statistical concepts, design and analysis of clinical trials, ethics, regulatory issues, and methodologies for clinical data management and analysis
Author: Ralph B. D'Agostino
Publisher:
ISBN:
Category : Clinical trials
Languages : en
Pages : 0
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Book Description
Author: Ralph B. D'Agostino
Publisher:
ISBN:
Category : Clinical trials
Languages : en
Pages : 0
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Book Description
Author: Lisa Marie Sullivan
Publisher: Wiley-Blackwell
ISBN:
Category : Biomedical engineering
Languages : en
Pages : 570
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Book Description
Here you'll find more than 500 entries from the world's leading experts in the field on the basic concepts, methodologies, and applications in clinical trials. The range of topics includes: basic statistical concepts, design and analysis of clinical trials, ethics, regulatory issues, and methodologies for clinical data management and analysis
Author: Ralph B. D'Agostino
Publisher: Wiley-Interscience
ISBN: 9780471352037
Category : Reference
Languages : en
Pages : 0
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Book Description
This monumental reference on all facets of clinical trials provides comprehensive coverage and emphasis on clearly stated and defined concepts, methodologies, and applications. With more than 450entries, from 350 of the world's leading experts in the field in academic and corporate settings, Encyclopedia of Clinical Trials is a world-class and one-of-a-kind compendia of basic concepts, methodologies, and applications in clinical trials. It includes coverage of: overview and basic statistical concepts; concepts of design and analysis of clinical trials; and methodologies and issues for clinical data analysis.
Author: Ralph B. D'Agostino
Publisher:
ISBN: 9781780342399
Category : Clinical trials
Languages : en
Pages :
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Book Description
This monumental reference on all facets of clinical trials provides comprehensive coverage and emphasis on clearly stated and defined concepts, methodologies, and applications.
Author: Jen-pei Liu
Publisher:
ISBN: 9780471462422
Category :
Languages : en
Pages : 0
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Book Description
Author: Narayanaswamy Balakrishnan
Publisher: John Wiley & Sons
ISBN: 1118595912
Category : Medical
Languages : en
Pages : 937
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Book Description
A complete guide to the key statistical concepts essential for the design and construction of clinical trials As the newest major resource in the field of medical research, Methods and Applications of Statistics in Clinical Trials, Volume 1: Concepts, Principles, Trials, and Designs presents a timely and authoritative reviewof the central statistical concepts used to build clinical trials that obtain the best results. The referenceunveils modern approaches vital to understanding, creating, and evaluating data obtained throughoutthe various stages of clinical trial design and analysis. Accessible and comprehensive, the first volume in a two-part set includes newly-written articles as well as established literature from the Wiley Encyclopedia of Clinical Trials. Illustrating a variety of statistical concepts and principles such as longitudinal data, missing data, covariates, biased-coin randomization, repeated measurements, and simple randomization, the book also provides in-depth coverage of the various trial designs found within phase I-IV trials. Methods and Applications of Statistics in Clinical Trials, Volume 1: Concepts, Principles, Trials, and Designs also features: Detailed chapters on the type of trial designs, such as adaptive, crossover, group-randomized, multicenter, non-inferiority, non-randomized, open-labeled, preference, prevention, and superiority trials Over 100 contributions from leading academics, researchers, and practitioners An exploration of ongoing, cutting-edge clinical trials on early cancer and heart disease, mother-to-child human immunodeficiency virus transmission trials, and the AIDS Clinical Trials Group Methods and Applications of Statistics in Clinical Trials, Volume 1: Concepts, Principles, Trials, and Designs is an excellent reference for researchers, practitioners, and students in the fields of clinicaltrials, pharmaceutics, biostatistics, medical research design, biology, biomedicine, epidemiology,and public health.
Author: Susan S. Ellenberg
Publisher: John Wiley & Sons
ISBN: 0470854154
Category : Mathematics
Languages : en
Pages : 208
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Book Description
There has been substantial growth in the use of data monitoring committees in recent years, by both government agencies and the pharmaceutical industry. This growth has been brought about by increasing recognition of the value of such committees in safeguarding trial participants as well as protecting trial integrity and the validity of conclusions. This very timely book describes the operation of data monitoring committees, and provides an authoritative guide to their establishment, purpose and responsibilities. * Provides a practical overview of data monitoring in clinical trials. * Describes the purpose, responsibilities and operation of data monitoring committees. * Provides directly applicable advice for those managing and conducting clinical trials, and those serving on data monitoring committees. * Gives insight into clinical data monitoring to those sitting on regulatory and ethical committees. * Discusses issues pertinent to those working in clinical trials in both the US and Europe. The practical guidance provided by this book will be of use to professionals working in and/or managing clinical trials, in academic, government and industry settings, particularly medical statisticians, clinicians, trial co-ordinators, and those working in regulatory affairs and bioethics.
Author: Shein-Chung Chow
Publisher: John Wiley & Sons
ISBN: 0471473294
Category : Mathematics
Languages : en
Pages : 754
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Book Description
Praise for the First Edition of Design and Analysis of Clinical Trials "An excellent book, providing a discussion of the clinical trial process from designing the study through analyzing the data, and to regulatory requirement . . . could easily be used as a classroom text to understand the process in the new drug development area." –Statistical Methods in Medicine A complete and balanced presentation now revised, updated, and expanded As the field of research possibilities expands, the need for a working understanding of how to carry out clinical trials only increases. New developments in the theory and practice of clinical research include a growing body of literature on the subject, new technologies and methodologies, and new guidelines from the International Conference on Harmonization (ICH). Design and Analysis of Clinical Trials, Second Edition provides both a comprehensive, unified presentation of principles and methodologies for various clinical trials, and a well-balanced summary of current regulatory requirements. This unique resource bridges the gap between clinical and statistical disciplines, covering both fields in a lucid and accessible manner. Thoroughly updated from its first edition, the Second Edition of Design and Analysis of Clinical Trials features new topics such as: Clinical trials and regulations, especially those of the ICH Clinical significance, reproducibility, and generalizability Goals of clinical trials and target population New study designs and trial types Sample size determination on equivalence and noninferiority trials, as well as comparing variabilities Also, three entirely new chapters cover: Designs for cancer clinical trials Preparation and implementation of a clinical protocol Data management of a clinical trial Written with the practitioner in mind, the presentation assumes only a minimal mathematical and statistical background for its reader. Instead, the writing emphasizes real-life examples and illustrations from clinical case studies, as well as numerous references-280 of them new to the Second Edition-to the literature. Design and Analysis of Clinical Trials, Second Edition will benefit academic, pharmaceutical, medical, and regulatory scientists/researchers, statisticians, and graduate-level students in these areas by serving as a useful, thorough reference source for clinical research.
