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You are here > Home > Reading Lists > Information Systems, Medical Records  & Technology Books > eClinical Trials Planning & Implementation

eClinical Trials: Planning and Implementation
Rebecca Daniels Kush, PhD, Paul Bleicher, MD, Stephen Raymond, PhD, Wayne Kubich, Ronald Marks, Barbara Tardiff

Softcover, 200 pages   
ISBN 193062428X
CenterWatch / Thomson Healthcare
May 2003
Price: $35.00
(Amazon may reduce this price for you)

 

This manual - the first-of-its-kind - is an invaluable resource designed to assist clinical trials programs, biopharmaceutical companies, CROs and investigative sites in understanding, planning and implementing electronic clinical trial (eCT) technology solutions to accelerate and improve their research operations. 

"This work...provides clear and insightful vision for integrated systems that share data to support all clinical trial operations." - Meredith Nahm, Director, Clinical Data Integration, Duke Clinical Research Institute, Board Member, Society for Clinical Data Management

Written by highly respected and authoritative thought leaders in the field today, this book describes and addresses the concepts and complexities of managing and conducting an optimal eCT, while offering practical guidance, facts and advice on implementing eCT technologies.

eClinical Trials: Planning and Implementation is routinely referenced by scientific, administrative and clinical IS personnel when planning and implementing eCT technology strategies.

"A truly outstanding and major contribution to drug development...I'm sure the book will fly off the shelves." - Dr. Elliot Danforth, Clinical Investigator, University of Vermont

This book assists you in:

  • Understanding how eCT technology solutions can accelerate and improve clinical research processes
  • Identifying ways to redesign the research processes in order to optimize the advantages of various eCT technologies
  • Considerations for establishing quantitative metrics to measure and track the impact of eCT technology implementation
  • Understanding and applying the intent of 21CFR11 and data privacy requirements
  • Comprehending the value of data interchange standards and how to ensure high quality data for clinical trials

"This work...provides clear and insightful vision for integrated systems that share data to support all clinical trial operations." - Meredith Nahm, Director, Clinical Data Integration, Duke Clinical Research Institute, Board Member, Society for Clinical Data Management

This book is perfect for:

  • Healthcare managers and physicians
  • Investigators, study nurses, pharmacists and other research professionals
  • CIOs and technology professionals
  • Instructors conducting training and educational programs
  • Sponsors, CROs, SMOs and academic institutions conducting clinical trials

You may also be interested in the book How to Grow Your Investigative Site.

(information provided by the publisher)

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