Category: OCR
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From the Office for Clinical Research
New Requirements for Enrolling Study Participants in ERMS!! As you know, each study team is responsible for entering all study enrollees into ERMS on the same day the patient signs the initial informed consent document. This is done for 2 reasons: Patient Safety: Entering subjects in ERMS triggers OCR staff to register subjects in PowerTrials, which triggers the…
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Tips to Speed up Your Clinical Trials Approvals
The Office of Sponsored Programs (OSP), the Office for Clinical Research (OCR), and the Institutional review Board (IRB) collaborated to document the most common causes of delays in clinical trial approvals at Emory. As a result of this collaboration, OSP, OCR, and the IRB have created the following “Tip Sheet” as a resource for departmental…