Clinical
Research Billing (CRB) is a very complex process that depends on a multitude of
factors to align in order to be compliant. Organizations with clinical research
activity face the challenge of maintaining a compliant CRB program without
adversely impacting patients. This web seminar will explain the process of
analyzing patient denials for trends related to participation in a clinical
research study and leveraging this information to influence the coverage
determination during the Medicare Coverage Analysis (MCA) process. Participants
will learn a 360 approach to increasing CRB compliance and reducing the burden
to the patients participating in clinical research studies.
- Describe the dynamics of the MCA process
- Explain the impact of MCA on patient billing and the revenue cycle
- Understand denials management and identify trends
- Apply denials management into the MCA process
- Analysts involved in the Medicare Coverage
Analysis process
- Study Coordinators
- Managers of Clinical Research Billing
Mary
L. Veazie, M.B.A., CPA, CHC, CHRC
Click here for complete trainer
biographies
$835
Includes up to 20 participants
at one site. 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 sites, please call +1
781.972.5400 or toll-free in the U.S. 800.856.2556 for pricing.
Barnett International is
accredited by the Accreditation Council for Pharmacy Education as a provider of
continuing pharmacy education. Participants will receive 2 hours
(0.2 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#: 0778-0000-18-062-L01-P.
Released: 9/18.
Hold
this course at your company! For more information, contact Naila Ganatra at +1
215.413.2471.