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 moreThe 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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