Course Description
Frequently, clinical research financial regulations, the budget process, clinical trial revenue cycle, and patient remuneration are obscure topics to not only the investigator, but also to the study team delegates. This web seminar describes the significance of ensuring that the investigator and study team are integrated into the financial components of the study to mitigate the risks associated with non-compliance with federal research billing regulations. Strategies for developing operational efficiencies and establishing communication channels to enhance sponsor reimbursements while reducing insurance denials will also be discussed.
Learning Objectives
Who Should Attend
Instructor
Mary L. Veazie, M.B.A., CPA, CHC, CHRC
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Registration Fees
$735*
*Includes up to 20 participants per login at a single location. All participants (up to 20) are eligible for “Certificates of Attendance,” and accreditation, provided that accreditation requirements are met. For groups larger than 20 or for additional logins for other locations, please call +1 781.972.5400 or toll-free in the U.S. 800.856.2556, or email customer.service@barnettinternational.com for pricing.
Accreditation Information
Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Participants will receive 1.5 hours (0.15 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation. Barnett International will issue a receipt of completion for earned CEUs within three weeks of program completion. ACPE#: 0778-0000-24-045-L99-P. Released: 9/24.
Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.