Cancer Protocol Review Committee (CPRC)
Access Requirements for CPRC Submission
OnCore access is required to submit to the CPRC.
(for all applications except Expedited)
- Applications must be submitted via ePRMS in OnCore.
- PIs are responsible for completing PI Signoff in the ePRMS console by logging into OnCore (required for all applications except Expedited and Amendments). This cannot be done by study staff on their behalf.
- If your OnCore password has expired or you require OnCore training, please contact firstname.lastname@example.org or 612-626-3080. The CPRC does not provide OnCore technical support or training. See the OnCore new user request form here.
MCC REDCap Subject Registration Template
To import the UMN MCC Subject Registration Template for your project:
- From the Online Designer page in a project, click on the button to "Import a new instrument from the official REDCap Shared Library".
- Once the shared library page is displayed, enter "UMN" (without the quotes) into the Keyword Search box and click on the "Search the library" button.
- Click on the link titled If you click on that then it will give you information about it and have links to see it as a web page, view it as a PDF, or "Import into my REDCap project". The last one is the one that will add it to your existing project.
This template must be used on all studies approved by the CPRC which select REDCap as their database
Interaction with IRB
The responsibilities of the Institutional Review Board (IRB) and the Cancer Protocol Research Committee (CPRC) are distinct. The CPRC operates independently from the IRB. The CPRC collaborates with the IRB to assure a minimum of administrative overlap.
- The CPRC responsibility is that of scientific review and prioritization.
- Review of consents and risk/benefit assessments are the purview of the IRB.
- Issues of risk may be discussed within the CPRC, but do not form the basis of Committee approval/disapproval.
- Clinical cancer research protocols approved by the CPRC will be reviewed for safety, ethical considerations and quality control by the IRB.
Clinical cancer research protocols may be submitted simultaneously to the IRB for pre-review but will not be reviewed by the IRB committee until CPRC approval is granted.
Approval by the CPRC and the IRB is required before any cancer-related clinical research protocol is activated.