Clinical Trials Risk Management
Published on 12. October 2005
232 pages
978-1-040-16958-2 (ISBN)
Description
Drug development is risky business. It is against the backdrop of huge financial, scientific, technical and medical risks that a clinical trials manager is expected to function, effectively identifying and managing all project risks, to deliver a successful outcome. Focusing on the day-to-day needs of a clinical trials manager, Clinical Trials Risk
Reviews / Votes
"...fills a key niche as there are few concise books offering a practical, readable guide to risk management."-Institute of Clinical Research
"A practical, readable guide, the book is packed with information that can be put to immediate use to improve current or planned clinical trials."
--Anticancer Research
"...a welcome addition to the clinical researcher's essential reading list...The book is well organized and, for a technical subject, easy to read, helped enormously by the use of humourous illustrations that gently emphasize the points being made...I can recommend this book to everyone working at the sharp end of clinical drug development."
-Good Clinical Practice Journal
More details
Language
English
Place of publication
London
United Kingdom
Publishing group
Taylor & Francis Ltd
Target group
Professional and scholarly
File size
13,37 MB
ISBN-13
978-1-040-16958-2 (9781040169582)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Classification
Other editions
Additional editions
Martin Robinson | Simon Cook
Clinical Trials Risk Management
Book
10/2005
1st Edition
CRC Press
€261.00
Shipment within 15-20 days
Persons
Content
Definitions and Concepts. Drug Safety and Pharmacovigilance. Types of Risk in Clinical Trials. Risk Identification. Threats and Opportunities. Planning Preventative Strategies. Backup Planning. Tracking Risks. Investigational Site Risk Management. Post Projection Evaluation.
