BOOK Data Monitoring Committees In Clinical Trials - A Practical Perspective by Susan S. Ellenberg [PDF ePUB Audiobook] Online

Free download and read ebooks online Data Monitoring Committees In Clinical Trials - A Practical Perspective by Susan S. Ellenberg, Thomas R. Fleming, David L. DeMets full book PDF ePUB Audiobook. Download a free ebooks and kindle audiobook Data Monitoring Committees In Clinical Trials - A Practical Perspective with ISBN id 9780471489863 full page with book summary. Susan S. Ellenberg book PDF ePUB of Data Monitoring Committees In Clinical Trials - A Practical Perspective published by Wiley in 2002-08-30. Data Monitoring Committees in Clinical Trials released with category Mathematics with total 208 pages.

Data Monitoring Committees In Clinical Trials - A Practical Perspective
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📖 Data Monitoring Committees In Clinical Trials - A Practical Perspective by Susan S. Ellenberg free pdf book

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.

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