The CRA's Guide to Monitoring Clinical Research is a valuable and practical educational resource for the individual readers and for group and staff training programs. Written by Karen E. Woodin, Ph.D., and John C. Schneider, this 400+ page CE-accredited book is an ideal resource for novice and experienced CRAs, as well as professionals interested in pursuing a career as study monitors. 
The CRA's Guide explains the role and responsibilities of a CRA, informs readers of the history of the regulations, explains in detail the research process and describes the regulations and GCPs that govern clinical research. 
Book topics: 
- Preparing for a study and selecting investigators - Obtaining and monitoring informed consent - Preparing for a monitoring visit - Recruiting and retaining study subjects - Conducting adverse event and safety monitoring - Preparing for audits and detecting fraud

The CRA's Guide to Monitoring Clinical Research

Medical Books

Schneider, John C.

Woodin, Karen E., Ph.D.

Research

CenterWatch

The CRC's Guide to Coordinating Clinical Research is a comprehensive training resource for investigative site staff. This invaluable guide offers CRCs the information they need to successfully coordinate a clinical trial from study startup to closeout and beyond. Topics covered include: *Developing standard operating procedures (SOPs) *Recruiting and retaining study subjects *Understanding the informed consent process *Working with protocols and case report forms *Recognizing adverse events *Preparing for audits The CRC's Guide to Coordinating Clinical Research is recommended for: *Novice and experienced CRCs *Professionals interested in getting involved with clinical research at the investigative site level *Investigative site staff

The CRC's Guide To Coordinating Clinical Research

CenterWatch, Inc.

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.

The CRA's Guide to Monitoring Clinical Research :2nd Edition

Medicine

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Books by Woodin, Karen E., Ph.D.