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Statistical Thinking for Non-Statisticians in Drug Regulation de Richard Kay

Descripción - Reseña del editor Statistical Thinking for Non-Statisticians in Drug Regulation, Second Edition, is a need-to-know guide to understanding statistical methodology, statistical data and results within drug development and clinical trials. It provides non-statisticians working in the pharmaceutical and medical device industries with an accessible introduction to the knowledge they need when working with statistical information and communicating with statisticians. It covers the statistical aspects of design, conduct, analysis and presentation of data from clinical trials in drug regulation and improves the ability to read, understand and critically appraise statistical methodology in papers and reports. As such, it is directly concerned with the day-to-day practice and the regulatory requirements of drug development and clinical trials. Fully conversant with current regulatory requirements, this second edition includes five new chapters covering Bayesian statistics, adaptive designs, observational studies, methods for safety analysis and monitoring and statistics for diagnosis. Authored by a respected lecturer and consultant to the pharmaceutical industry, Statistical Thinking for Non-Statisticians in Drug Regulation is an ideal guide for physicians, clinical research scientists, managers and associates, data managers, medical writers, regulatory personnel and for all non-statisticians working and learning within the pharmaceutical industry. Contraportada Statistical Thinking for Non-Statisticians in Drug Regulation, Second Edition, is a need-to-know guide to understanding statistical methodology, statistical data and results within drug development and clinical trials.It provides non-statisticians working in the pharmaceutical and medical device industries with an accessible introduction to the knowledge they need when working with statistical information and communicating with statisticians. It covers the statistical aspects of design, conduct, analysis and presentation of data from clinical trials in drug regulation and improves the ability to read, understand and critically appraise statistical methodology in papers and reports. As such, it is directly concerned with the day-to-day practice and the regulatory requirements of drug development and clinical trials.Fully conversant with current regulatory requirements, this second edition includes five new chapters covering Bayesian statistics, adaptive designs, observational studies, methods for safety analysis and monitoring and statistics for diagnosis.Authored by a respected lecturer and consultant to the pharmaceutical industry, Statistical Thinking for Non-Statisticians in Drug Regulation is an ideal guide for physicians, clinical research scientists, managers and associates, data managers, medical writers, regulatory personnel and for all non-statisticians working and learning within the pharmaceutical industry. Biografía del autor Richard Kay, Consultant in Statistics for the Pharmaceutical Industry, Great Longstone, Derbyshire, UK

Detalles del Libro

Name: Statistical Thinking for Non-Statisticians in Drug Regulation
Autor: Richard Kay
Categoria: Libros,Libros universitarios y de estudios superiores,Medicina y ciencias de la salud
Tamaño del archivo: 10 MB
Tipos de archivo: PDF Document
Idioma: Español
Archivos de estado: AVAILABLE

[Download] Statistical Thinking for Non-Statisticians in Drug Regulation de Richard Kay libros ebooks

Statistical Thinking for Non‐Statisticians in Drug ~ Statistical Thinking for Non-Statisticians in Drug Regulation, Second Edition, is a need-to-know guide to understanding statistical methodology, statistical data and results within drug development and clinical trials. It provides non-statisticians working in the pharmaceutical and medical device industries with an accessible introduction to the knowledge they need when working with .

Statistical Thinking for Non-Statisticians in Drug ~ Statistical Thinking for Non-Statisticians in Drug Regulation, Second Edition, is a need-to-know guide to understanding statistical methodology, statistical data and results within drug development and clinical trials. It provides non-statisticians working in the pharmaceutical and medical device industries with an accessible introduction to the knowledge they need when working with .

Statistical Thinking for Non-Statisticians in Drug Regulation ~ Statistical thinking for non-statisticians in drug regulation / Richard Kay. – Second edition. p. ; cm. Includes bibliographical references and index. ISBN 978-1-118-47094-7 (cloth) I. Title. [DNLM: 1. Clinical Trials as Topic–methods. 2. Drug Approval. 3. Drug Industry. 4. Statistics as Topic. QV 771.4] R853.C55 615.5′80724–dc23 2014020541

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Statistical Thinking for Non-Statisticians in Drug ~ Statistical Thinking for Clinical Trials in Drug Regulation presents the concepts and statistical thinking behind medical studies with a direct connection to the regulatory environment so that readers can be clear where the statistical methodology fits in with industry requirements.

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Statistical Thinking for Non Statisticians in Drug ~ Statistical Thinking for Non Statisticians in Drug Regulation Book Based on the course with the same title this highly regarded book, now in its second edition, provides a clear, comprehensive and accessible guide to statistics for the non-statistician working in the pharmaceutical industry.

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Statistical Thinking for Non–Statisticians in Drug Regulation ~ Statistical Thinking For Non–Statisticians In Drug Regulation è un libro di Kay Richard edito da Wiley–Blackwell a ottobre 2014 - EAN 9781118470947: puoi acquistarlo sul sito HOEPLI, la grande libreria online.

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Statistical Thinking for Non-Statisticians in Drug Regulation ~ Statistical Thinking for Non-Statisticians in Drug Regulation Statistical Thinking for Non-Statisticians in Drug Regulation Richard Kay Consultant in Statistics for the Pharmaceutical Industry Great Longstone Derbyshire, UK

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