How do you judge the success of a clinical trial? By traditional measures, certainly: it must be completed on or ahead of schedule, at or under budget, with all deliverables meeting accepted levels of quality.
The process starts with the end firmly in mind using IICRT Planning. We look at feasibility — is what we’re considering even possible? — and at developing the protocol, identifying risks, and mapping out the timeline. Next, IICRT Start kicks off study planning, personnel training, vendor selection, planning of monitoring options, and systems set-up.
IICRT Drive is all about process and accountability. Quality control, data surveillance, resource coordination, risk mitigation — if it promotes scientific rigor and ensures trial integrity, we’re on top of it. Finally, IICRT Finish distills a mountain of data into information that’s meaningful and helps answer the question that awaits at every study’s conclusion: “What’s next?”