Incorporating Denials Management into Clinical Research Billing

Oct 6, 2018, 18:23 PM
Course ID : 247
Acronym : CTF
Streamline your clinical research billing process with denials management strategies. Enroll now at Barnett International.

Course Description

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.

Learning Objectives

  • 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

Who Should Attend

  • Analysts involved in the Medicare Coverage Analysis process
  • Study Coordinators
  • Managers of Clinical Research Billing

Instructor

Mary L. Veazie, M.B.A., CPA, CHC, CHRC

Click here for complete trainer biographies

Registration Fees

$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.

Note: Due to COVID-19, we understand that most teams cannot currently dial-in together. As such, we are able to offer additional logins at a highly reduced rate. Please contact Barnett Customer Service at +1 781.972.5400 or toll-free in the U.S. 800.856.2556 to register with your additional participants requiring login credentials. Or email Customer Service at: customer.service@barnettinternational.com 

Accreditation Information

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#: 0778-0000-24-021-L99-P. Released: 6/24. 

Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.

Series :
  • Clinical Trials & Translational Medicine
Topics :
  • Clinical Research
  • Drug Safety & Development
  • Medical Device
  • Project Management
  • Regulatory Compliance
Job Functions :
  • Clinical Operations & Trial Management
  • Clinical Quality Assurance
  • Clinical Research Associate
  • Clinical Research Coordinator
  • Clinical Research Investigator
  • Data Management
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