Sponsored by the MGH Divison of Clinical Research and the MGH Office of Research Compliance
Speaker: Pamela Richtmyer, Senior Research Compliance Associate, MGH Research Compliance
This presentation will provide a basic overview of clinical research billing. Attendees will gain a general understanding of the clinical research billing process including:
•Developing a study budget that will cover all costs
•Determining what is billable to insurance
•Routing charges appropriately
•Maintaining financial health of study
•Understanding relevant regulations and requirements
• Available resources
This course is geared towards investigators, research nurses, study coordinators, and all other study staff.
This program meets the requirements of the Board of Registration in Nursing, at 244 CMR 5.00, for 1 contact hour of nursing continuing education.
Registration is required. Contact dcredu@partners.org with further questions about this session.
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The rest of the Clinical Trial Billing Educational Series schedule is listed below.
•Clinical Trial Billing (Part 2): Tracking Charges and Patient Care Corrections
•Clinical Trial Billing (Part 3): Special Considerations – MCAs and Devices
Sponsor: MGH Division of Clinical Research
Modules
| Clinical Trials Billing: Basic Overview (Part 1) |
Past Offerings
| Clinical Trials Billing: Basic Overview (Part 1) | Sept. 27, 2016 |