Описание: READ ALL ABOUT IT! David Spiegelhalter has recently joined the ranks of Isaac Newton, Charles Darwin and Stephen Hawking by becoming a fellow of the Royal Society. Originating from the Medical Research Council`s biostatistics unit, David has played a leading role in the Bristol heart surgery and Harold Shipman inquiries.
Описание: This book provides an up--to--date, comprehensive, clinically oriented account of the molecular biology, pathogenesis, clinical features, diagnosis and management of human bacterial diseases, as well as their control and prevention.
Автор: DeMets Название: Data Monitoring in Clinical Trials ISBN: 0387203303 ISBN-13(EAN): 9780387203300 Издательство: Springer Рейтинг: Цена: 10760.00 р. Наличие на складе: Есть у поставщика Поставка под заказ.
Описание: Randomized clinical trials are the standard for establishing clinical practice guidelines and are central to evidence based medicine. The trials must be monitored for recruitment progress, quality of data, and adherence to patient care or prevention standards. This book illustrates the complexity of this monitoring process.
Автор: Hulley Название: Designing clinical research ISBN: 1608318044 ISBN-13(EAN): 9781608318049 Издательство: Lippincott Williams & Wilkins Рейтинг: Цена: 12355.00 р. Наличие на складе: Нет в наличии.
Описание: Designing Clinical Research has been extensively revised and continues to set the standard as a practical guide for doctors, nurses, pharmacists, and other health professionals involved in all forms of clinical, translational, and public health research. It presents advanced epidemiologic concepts in a reader-friendly way, and suggests common sense approaches to the challenging judgments involved in designing, funding, and implementing. New to this edition: Expanded and updated content in every chapter, with new material on: • non-inferiority trials for comparative effectiveness research • incidence-density case-control studies • confounding and effect modification • diagnostic test studies to inform prediction rules • ethical aspects of whole genome sequencing • automated data management approaches • new NIH grant-writing requirements Color format, and Electronic access, powered by Inkling™ as a free companion to the text • viewable through your browser or as a download to tablet or smartphone • the complete text with optimized navigation • note-sharing, highlighting and bookmarking capability • cross-linking of references and content • rapid search options linked to the new glossary
Описание: Provides a practical approach for dealing with the legal and regulatory compliance issues involved in human research. Covering a range of topics, such as consent, confidentiality, subject recruitment and selection, and Institutional Review Board, this book offers useful strategies for achieving regulatory compliance while reducing liability.
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