Management of Data in Clinical Trials (Wiley Series in Probability and Statistics) - Hardcover

Buch 162 von 354: Wiley Series in Probability and Statistics

McFadden, Eleanor

 
9780471303169: Management of Data in Clinical Trials (Wiley Series in Probability and Statistics)

Inhaltsangabe

This book explores data management-from study development to final analysis-and suggests alternative approaches, with guidelines on optimal approaches under various circumstances. It discusses different approaches to clinical trials for some of the major diseases and compares approaches in the U.S. and Europe.

Die Inhaltsangabe kann sich auf eine andere Ausgabe dieses Titels beziehen.

Über die Autorin bzw. den Autor

ELEANOR McFADDEN is Director of the Coordinating Center for the Eastern Cooperative Oncology Group at Frontier Science and Technology Research Foundation, Brookline, Massachusetts. She has been involved in clinical trials data management for twenty years and has published articles and taught courses on various aspects of trial management.

Von der hinteren Coverseite

Timely, authoritative, complete-a comprehensive guide to managing data in clinical trials

At some point during their training, virtually all health professionals are exposed to the theory of clinical trials, but few are taught about the practical details of organizing and conducting a clinical trial. This book fills that gap in training.

Management of Data in Clinical Trials is a valuable working resource for anyone involved in any type of clinical trial-from large multicenter trials to small single-investigator studies. The information is relevant to trials in all disease areas, done in any clinical setting, and is general enough to be applicable both within and outside the United States. This authoritative handbook offers in-depth coverage of accrual and follow-up phases of a clinical trial and provides valuable expert advice and step-by-step guidance on:
* Trial planning and resource assessment
* Developing a trial protocol and case report forms
* Selection and use of computers and software for clinical trials
* Eligibility checking and patient registration
* Data collection and data entry
* Quality control systems at the local and central levels
* Training and education of data management staff
* The role of data management in implementing good clinical practice (GCP)
* Development of software tools for trial management

„Über diesen Titel“ kann sich auf eine andere Ausgabe dieses Titels beziehen.