The CRA's Guide to Monitoring Clinical Research, Third Edition [Perfect Paperback]
Author: Karen E. Woodin Ph.D. John C. Schneider Cheryl Rosenfeld | Language: English | ISBN: 1930624603 | Format: PDF, EPUB
The CRA's Guide to Monitoring Clinical Research, Third Edition
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Posts about Download The Book The CRA's Guide to Monitoring Clinical Research, Third Edition [Perfect Paperback] from 4shared, mediafire, hotfile, and mirror link
The CRA's Guide to Monitoring Clinical Research, now in its third edition, continues to be a key resource for both novice and experienced CRAs seeking to learn more about the field of monitoring or to better understand their roles and responsibilities as the industry becomes more global and technologically focused. With helpful tips and strategies, checklists, personal experiences, key takeaways and exercises, plus new chapters on clinical trial roles and responsibilities, monitoring for device and biologic trials, globalization of studies, EDC and more, The CRA's Guide is a must-have training and educational tool that you ll refer to again and again.
Topics include: -A comprehensive review of CRA roles and responsibilities
-Understanding regulations and GCPs
-Study initiation and monitoring plans
-Recruiting and retaining study subjects -The informed consent process
-Conducting adverse event and safety monitoring
-Preparing for audits and detecting fraud
-The future outlook
-Job descriptions and current academic programs
-Devices and Biologics
-Managing Multi-national Trials
-IRBs and Data Safety Monitoring Boards
-Exercises with Answers
Recommended for: -Novice and experienced CRAs
-Health professionals interested in pursuing a career as a study monitor
-Instructors conducting training and educational programs
Books with free ebook downloads available The CRA's Guide to Monitoring Clinical Research, Third Edition Topics include: -A comprehensive review of CRA roles and responsibilities
-Understanding regulations and GCPs
-Study initiation and monitoring plans
-Recruiting and retaining study subjects -The informed consent process
-Conducting adverse event and safety monitoring
-Preparing for audits and detecting fraud
-The future outlook
-Job descriptions and current academic programs
-Devices and Biologics
-Managing Multi-national Trials
-IRBs and Data Safety Monitoring Boards
-Exercises with Answers
Recommended for: -Novice and experienced CRAs
-Health professionals interested in pursuing a career as a study monitor
-Instructors conducting training and educational programs
- Perfect Paperback: 678 pages
- Publisher: CenterWatch; Third edition (July 5, 2011)
- Language: English
- ISBN-10: 1930624603
- ISBN-13: 978-1930624603
- Product Dimensions: 1.5 x 6 x 9 inches
- Shipping Weight: 2.4 pounds (View shipping rates and policies)
- Amazon Best Sellers Rank: #168,419 in Books (See Top 100 in Books)
I was worried that I was paying too much for this book and that I wouldn't get much out of it, I was SOOOO wrong.By Jessica Gallagher
I've been a CRA for over 8 years now and read the first edition of the CRA's guide as well. This new (third) edition is awesome!
The best one yet! The content section in the back is great! The tables are a great reference. I would definitely recommend this book to anyone looking to become a CRA as well as the experienced CRA. It's a great tool to have around.
This book provides a thorough understanding and overview into clinical research. I would recommend this book to anyone who is considering this career path.By Quanya Harris
i cannot download it
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