A Practical Guide to Managing Clinical Trials

Joann Pfeiffer

ISBN 10: 0367497824 / ISBN 13: 9780367497828

Published by CRC Press, 2020

About this Item

nach der Bestellung gedruckt Neuware - Printed after ordering - A Practical Guide to Managing Clinical Trials is a basic, comprehensive guide to conducting clinical trials. Designed for individuals working in research site operations, this user-friendly reference guides the reader through each step of the clinical trial process from site selection, to site set-up, subject recruitment, study visits, and to study close-out. Topics include staff roles/responsibilities/training, budget and contract review and management, subject study visits, data and document management, event reporting, research ethics, audits and inspections, consent processes, IRB, FDA regulations, and good clinical practices. Each chapter concludes with a review of key points and knowledge application.Unique to this book is 'A View from India,' a chapter-by-chapter comparison of clinical trial practices in India versus the U.S. Throughout the book and in Chapter 10, readers will glimpse some of the challenges and opportunities in the emerging and growing market of Indian clinical trials.

Seller Inventory # 9780367497828

Bibliographic Details

• Title: A Practical Guide to Managing Clinical Trials
• Publisher: CRC Press
• Publication Date: 2020
• Language: English
• ISBN 10: 0367497824
• ISBN 13: 9780367497828
• Binding: Taschenbuch
• Condition: Neu
• Dimensions: 234W x 156H x 15D millimeters 234 millimeters width by 156 millimeters height by 15 millimeters depth
• Weight: 424 grams

About this title

Synopsis

A Practical Guide to Managing Clinical Trials is a basic, comprehensive guide to conducting clinical trials. Designed for individuals working in research site operations, this user-friendly reference guides the reader through each step of the clinical trial process from site selection, to site set-up, subject recruitment, study visits, and to study close-out. Topics include staff roles/responsibilities/training, budget and contract review and management, subject study visits, data and document management, event reporting, research ethics, audits and inspections, consent processes, IRB, FDA regulations, and good clinical practices. Each chapter concludes with a review of key points and knowledge application.

Unique to this book is "A View from India," a chapter-by-chapter comparison of clinical trial practices in India versus the U.S. Throughout the book and in Chapter 10, readers will glimpse some of the challenges and opportunities in the emerging and growing market of Indian clinical trials.

About the Author

Dr. JoAnn Pfeiffer has extensive experience in site management, and is currently the Program Director of Arizona State University’s (ASU) Clinical Research Management Program in the College of Nursing and Health Innovation.

Dr. Cris Wells has broad experience in overseeing basic and translational studies as well as clinical trials. She is currently the Senior Director of Health-Related Programs at ASU.