There are many steps that must be taken to assess risk and integrate quality when developing, initiating and conducting a clinical trial. These steps are crucial for every type of clinical trial. This session will describe how to apply those principles to investigator-initiated clinical trials utilizing tips, tools and templates available to help along the way.
Identify quality standards, and areas of risk, for clinical trials.
Describe measures to incorporate quality into study design and initiation of Investigator-Initiated Trials (IITs).
Examine ways to assess quality during IIT study conduct.