Start Up and OperationsDuke Early Phase Clinical Research internal processes and tools allow us to accelerate study start-up, IRB approval, and recruitment timelines.
Tools that permit us to query the Duke medical record system and a proprietary research volunteer registry give us the ability to rapidly identify suitable study candidates after the appropriate approvals have been obtained.
We are able to initiate the regulatory process in parallel with contracting negotiations to expedite the time between contract signature and a study’s institutional approval.
RSV Vaccine Study
DDI Vaccine Study