You consented a research patient. Did you notify UCI within 24 hours?
Notification within 24 hours of research subjects consenting to a clinical trial prevents fraudulent billing to patients or their insurance.
Here's how:
Upon consenting of a research subject into a clinical trial, you must register your research subject in the OnCore Clinical Trial Management System (CTMS) subject management console.
Completion of this activity will notify the Research Revenue Integrity (RRI) unit, and places a research flag on your subject’s accounts in Epic to prevent erroneous claims to patients or their insurance.
For more information, please see:
OnCore Clinical Trials Management
OnCore Training Request Form
If you have any questions, please contact Mary Alexander, Research Compliance Officer, at pargam@uci.edu or 714-456-8986.
Thank you,
Valerie M. Dixon, CCEP, CHC
Interim Chief Compliance & Privacy Officer
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