Register here at least 48 hours before the seminar start time
Synopsis
Clinical research billing and finance (CRBF) is frequently associated with industry-negotiated clinical trials, CRBF compliance applies to all research studies that include one or more prospective clinical services. This presentation will focus on pre- and post-award CRBF requirements, including budgeting, billing, and NIH policy requirements related to patient care costs, as well as studies that have no external funding.
Speakers
- Mike Porreca, Director, Clinical Trial Office (CTO), BUMC/BMC
- Sandy Lok, Contract Specialist, BMC
- Kaye Mottola, Research Policy and Education Manager, BMC
Learning Objectives:
By the end of the seminar, participants should be able to:
- Explain the operative definition of “clinical research” in CRBF
- Identify the full range of clinical research studies that are subject to CRBF requirements
- Discuss key features of CRBF compliance, and
- Locate resources for learning more about (or refreshing one’s memory of) the BMC/BU CRBF process.