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Considerations for Clinical Research Billing Compliance

Considerations for Clinical Research Billing Compliance

 

Objectives:
Review Clinical Research Billing Requirements
Define Coverage Analysis and Discuss Considerations During Development
Discuss Contract and Informed Consent Considerations
Discuss Risks and Consequences of Non-Compliance
Discuss General Barriers and Challenges Related to Clinical Research Billing

Date: 7/18/12, 12pm to 1pm
Time: 7/18/12, 12pm to 1pm
Location: FCT3.5001
Format: All Employee Meeting
CME: 1.0
Facilitator: Institutional Compliance
Speaker: Mikki O’Neal, MBA, CCRP, CCRC, CHRC
Speaker Bio: Mikki O’Neal, M.B.A., C.C.R.P., C.C.R.C., C.H.R.C., is a Manager in The University of Texas MD Anderson Cancer Center’s (MD Anderson’s) Institutional Compliance Office. In this role, Mikki is responsible for managing clinical research billing compliance activities on the Billing & Reimbursement Compliance team. Mikki joined MD Anderson and the Institutional Compliance Office in April of 2011.
Sponsor: Institutional Compliance
Contact: Julia Romero - jmromero@mdanderson.org

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