CRC Clinical Resources Application
The Process for New Application Submission
The CRC Clinical Resources Application is a compliance tool requesting the use of the center, its resources and the cores of the R-CENTER and Clinical Research Network (CRN).
A completed application must be submitted via the R-CENTER web portal to the Clinical Research Center (CRC) for approval by Scientific Advisory Council (SAC) and the CRC Medical Director prior to initiation of any clinical trial/protocol in the CRC.
The CRC Protocol Implementation Team meetings are held twice per month and applications will be screened at that time. A follow-up roundtable discussion will be scheduled within 7-10 business days.
A completed application must be submitted via the R-CENTER web portal to the Clinical Research Center (CRC) for approval by Scientific Advisory Council (SAC) and the CRC Medical Director prior to initiation of any clinical trial/protocol in the CRC.
The CRC Protocol Implementation Team meetings are held twice per month and applications will be screened at that time. A follow-up roundtable discussion will be scheduled within 7-10 business days.
