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Clinical Research Billing Compliance Education

Clinical Research Billing Compliance Education

Overview:

This course will provide the background of clinical research billing rules, documentation requirements for clinical research billing, and discuss the importance of effective communication, coordination, and collaboration between departments.
 
Objectives:
  • Review Clinical Research Billing Requirements- A refresher
  • Define Coverage Analysis (CA) and Discuss Considerations During Development
  • Discuss Contract, Budget and Informed Consent Development Considerations
  • Discuss Risks and Consequences of Non-Compliance
  • Discuss General Barriers and Challenges Related to Clinical Research Billing

Date: 9/27/12, 9:30am to 11:30am
Time: 9/27/12, 9:30am to 11:30am
Location: FCT3.5001
Format: All Employee Meeting
CME: 1.0
Speaker: Mikki O'Neal
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.
Contact: Julia Romero - (713) 563-0399 - jmromero@mdanderson.org

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