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Titlebook: Clinical Trials in Osteoporosis; Derek Pearson (Clinical Director),Colin G. Miller Book 20021st edition Springer-Verlag London 2002 Clini

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发表于 2025-3-21 19:50:22 | 显示全部楼层 |阅读模式
书目名称Clinical Trials in Osteoporosis
编辑Derek Pearson (Clinical Director),Colin G. Miller
视频video
概述Specifically addresses the issue of clinical trials in osteoporosis (no book on the subject is in the Library of Congress Catalog).Combines a number of issues that have been brought together for the f
图书封面Titlebook: Clinical Trials in Osteoporosis;  Derek Pearson (Clinical Director),Colin G. Miller  Book 20021st edition Springer-Verlag London 2002 Clini
描述.Clinical Trials in Osteoporosis. is a practical handbook on clinical trials in the growing field of osteoporosis. Topics covered include study design, technical issues, data collection, quality assurance, data analysis and presentation. It aims to take the user through the process step-by-step from start to finish, also providing a background on regulatory guidelines, ethical implications, endpoints, current therapies and the ideal drug to use..There are no other books at present that specifically address the issue of clinical trials in osteoporosis. A number of issues dealt with in this book have been brought together in one publication for the first time..Clinical Trials in Osteoporosis. is intended to serve as a practical manual for clinicians and scientists coming to the subject new and to provide a standard for existing centers to measure themselves against.
出版日期Book 20021st edition
关键词Clinical Trials; Instrument; Methodology; Study; bone; clinical trial; drug; osteoporosis
版次1
doihttps://doi.org/10.1007/978-1-4471-3710-8
isbn_ebook978-1-4471-3710-8
copyrightSpringer-Verlag London 2002
The information of publication is updating

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Conclusions and Future Actions,y the densitometer technologist who will be responsible for ensuring subject data is adequately acquired, principal investigators and study monitors have a role in ensuring that the technologist is adequately prepared and is included as a member of the clinical trial team. The preparation will include both relevant training and trial documentation
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https://doi.org/10.1007/978-3-642-54353-1 the International Committee for Harmonization (ICH) and adopted by the Food and Drug Administration (FDA) for the USA. and the Committee for Proprietary Medicinal Products (CPMP) within Europe.. These cover issues that researchers must consider, such as:
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Satellite Tracking and ObservationModels, the particular extras and details that have to be evaluated, and this chapter provides an overview of these items. The sponsor needs to be aware of these items in a timely manner — all too often the novice will overlook an important detail until it becomes a critical issue. This chapter will help ensure these kinds of errors are avoided.
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PSI Subsidence Monitoring in Groningen,ical area in its infancy, we can therefore expect a significant number of changes in the coming years, as the understanding of bone physiology becomes more comprehensive and the genetic factors leading to increased risk factors become known.
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Introductiont is understood by those working in it, but currently has no definition that is agreeable across the medical and scientific community and a poorly understood etiology. It is within this framework that the pharmaceutical industry is trying to develop new treatments for the so-called “silent epidemic”.
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Ethical Considerations the International Committee for Harmonization (ICH) and adopted by the Food and Drug Administration (FDA) for the USA. and the Committee for Proprietary Medicinal Products (CPMP) within Europe.. These cover issues that researchers must consider, such as:
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