Leveraging Clinical Research Processes to Decrease Denials

Instructor: Mary Veazie
Product ID: 706366
Training Level: Intermediate
  • Duration: 90 Min
This course will demonstrate 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 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.
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Why Should You Attend:

Clinical Research Billing (CRB) is a very complex process that depends on a multitude of factors to align to be compliant. Organizations with clinical research activity face the challenge of maintaining a complaint CRB program without adversely impacting its patients. This course will demonstrate 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 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.

Areas Covered in the Webinar:

  • History and purpose of the Medicare Coverage Analysis (MCA)
  • Uses of the MCA
  • Development of MCA
  • Overview of revenue cycle
  • Overview of clinical research billing
  • Understanding patient billing processes
  • Understanding denials
  • Leverage denials data to minimize loss revenue

Who Will Benefit:

  • Clinical Research Coordinators
  • Clinical Trial Managers
  • Clinical Research Associates
  • Clinical Research Managers/Directors
  • Administrative Directors
  • Financial Analysts

From:

  • Academic Medical Centers, Academic Universities involved in clinical research, community based hospitals

Free Materials:

  • Reference documents
  • Rule documents or guidance
  • Checklist
  • MCA template
  • Articles
Instructor Profile:
Mary Veazie

Mary Veazie
Executive Director, Clinical Research Finance

Mary Veazie is a Certified Public Accountant with over 15 years of experience in clinical research finance. Collectively, she has over 25 years of financial and auditing experience. She developed and directed a clinical research finance office for a large academic medical center. She is certified in Healthcare Research Compliance and Healthcare Compliance. Ms. Veazie’s skill set includes full comprehension of the clinical research billing process and its impact on an organization’s clinic operations and revenue cycle.

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Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

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