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Assessing Quality of Life in Clinical Trials, Fayers, Peter; Hays, Ron


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Цена: 147840.00T
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Автор: Fayers, Peter; Hays, Ron
Название:  Assessing Quality of Life in Clinical Trials
Перевод названия: Оценка качества жизни в клинических испытаниях
ISBN: 9780198527695
Издательство: Oxford Academ
Классификация:



ISBN-10: 0198527691
Обложка/Формат: Hardback
Страницы: 482
Вес: 0.98 кг.
Дата издания: 10.03.2005
Язык: English
Издание: 2 rev ed
Иллюстрации: Numerous tables
Размер: 240 x 168 x 31
Читательская аудитория: Professional & vocational
Подзаголовок: Methods and practice
Ссылка на Издательство: Link
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Поставляется из: Англии
Описание: Researchers in all clinical fields are fully aware of the importance of Quality of Life measurements in judging the efficacy of a given treatment. Psychological criteria play an important role in this evaluation. Assessing Quality of Life in Clinical Trials explores the current state of the art and illustrates the benefits and potential of health related quality of life assessment in clinical trials. It cover a wide range of analytical issues, emphasizing new and innovative approaches that are of practical and clinical importance. The book will have widespread appeal to clinical trialists and researchers from a wide range of specialties.
Дополнительное описание: Preface; 1. Developing and evaluating questionnaires; 1.1: Ron Hays: Generic versus disease-targeted instruments; 1.2: Elaine McColl: Developing questionnaires; 1.3: Ron Hays & Dennis Revicki: Reliability and validity, including responsi


Oxford Handbook of Clinical Pharmacy 2/e

Автор: Wiffen, Philip; Mitchell, Marc; Snelling, Melanie;
Название: Oxford Handbook of Clinical Pharmacy 2/e
ISBN: 0199603642 ISBN-13(EAN): 9780199603640
Издательство: Oxford Academ
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Цена: 36950.00 T
Наличие на складе: Поставка под заказ.
Описание: Now fully updated, the Oxford Handbook of Clinical Pharmacy remains the indispensible guide to clinical pharmacy, providing all the information needed for practising and student pharmacists. Presenting handy practical guidance in a quick-reference, bullet-point format, this handbook will supply the knowledge and confidence needed to provide a clinical pharmacy service. Complementing the current British National Formulary guidelines, the handbook gives prescribing points and linked concepts of relevance to clinical pharmacists. The contents are evidence-based and contain a wealth of information from the authors' many years of clinical pharmacy experience. This handbook is the definitive quick-reference guide for all practising and student pharmacists.

Bioequivalence and Statistics in Clinical Pharmacology

Автор: Patterson
Название: Bioequivalence and Statistics in Clinical Pharmacology
ISBN: 1584885300 ISBN-13(EAN): 9781584885306
Издательство: Taylor&Francis
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Цена: 87790.00 T
Наличие на складе: Нет в наличии.
Описание: Bioequivalence and Statistics in Clinical Pharmacology covers the applications and basic elements of the theory of statistical methods in clinical pharmacology. It establishes techniques used in the assessment of bioequivalence and describes the use of statistics in clinical pharmacology studies of safety, ECG monitoring, efficacy, and population pharmacokinetics. The authors demonstrate study design, analysis, and interpretation of data using real data examples. The book emphasizes regulatory applications related to drug development and features a wide range of datasets as well as SAS and SPLUS code available on the Internet.

Simulation For Designing Clinical Trials: A Pharmacokinetic-Pharmacodynamic Modeling Perspective

Автор: Kimko Hui
Название: Simulation For Designing Clinical Trials: A Pharmacokinetic-Pharmacodynamic Modeling Perspective
ISBN: 0824708628 ISBN-13(EAN): 9780824708627
Издательство: Taylor&Francis
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Цена: 183750.00 T
Наличие на складе: Есть у поставщика Поставка под заказ.
Описание: Providing more than just a comprehensive history, critical vocabulary, insightful compilation of motivations, and clear explanation of the state-of-the-art of modern clinical trial simulation, this book supplies a rigorous framework for employing simulation as an experiment, according to a predefined simulation plan, that reflects good simulation practices. The book discusses how to design clinical trials according to their probability for success, techniques to define distributions of virtual subjects' characteristics, methods to determine the sensitivity of the trial design, and the population relationship between dosing schedules and patient response.


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