The CRA's Guide to Monitoring Clinical Research :2nd Edition
ISBN-13:
9781930624559
ISBN-10:
1930624557
Edition:
2
Author:
Karen E. Woodin, John C. Schneider, Sara Gambrill, Steve Zisson
Publication date:
2008
Publisher:
Centerwatch Inc
Format:
Paperback
454 pages
Category:
Internal Medicine
,
Medicine
FREE US shipping
Book details
ISBN-13:
9781930624559
ISBN-10:
1930624557
Edition:
2
Author:
Karen E. Woodin, John C. Schneider, Sara Gambrill, Steve Zisson
Publication date:
2008
Publisher:
Centerwatch Inc
Format:
Paperback
454 pages
Category:
Internal Medicine
,
Medicine
Summary
The CRA's Guide to Monitoring Clinical Research :2nd Edition (ISBN-13: 9781930624559 and ISBN-10: 1930624557), written by authors
Karen E. Woodin, John C. Schneider, Sara Gambrill, Steve Zisson, was published by Centerwatch Inc in 2008.
With an overall rating of 4.2 stars, it's a notable title among other
Internal Medicine
(Medicine) books. You can easily purchase or rent The CRA's Guide to Monitoring Clinical Research :2nd Edition (Paperback) from BooksRun,
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Internal Medicine
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Description
The CRA's Guide to Monitoring Clinical Research is a comprehensive and practical educational resource for both the novice and experienced CRA. This newly updated training tool provides essential information on the clinical research process, regulations, role responsibilities, helpful hints and personal experiences. This guide also teaches CRAs to demonstrate how regulations, GCPs and SOPs can be applied to everyday operations of conducting and monitoring clinical trials.
Topics covered include:
*The history behind the regulations
*Clinical study preparation
*The informed consent process
*Adverse events and safety monitoring
*Recruitment, retention and compliance of study subjects
*Errors, misconduct and fraud
*The future of CRAs and more
The CRA's Guide to Monitoring Clinical Research is also recommended for CROs, clinical trial sponsors and investigative sites conducting group or staff training programs.
Topics covered include:
*The history behind the regulations
*Clinical study preparation
*The informed consent process
*Adverse events and safety monitoring
*Recruitment, retention and compliance of study subjects
*Errors, misconduct and fraud
*The future of CRAs and more
The CRA's Guide to Monitoring Clinical Research is also recommended for CROs, clinical trial sponsors and investigative sites conducting group or staff training programs.
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