Leveraging Clinical Research Processes to Decrease Denials
Instructor:
Mary Veazie
Product ID: 706366
Training Level: Intermediate
- Duration: 90 Min
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
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.
More Training By Experts
- Financial Management of Clinical Research: Developing Data Analytics to Drive Decision Making
- Introduction to Medicare Coverage Analysis - Impact on Revenue Cycle
- Claims Processing: Appropriate Segregation of Charges & Medical Documentation for Clinical Research Studies
- Streamlining Clinical Trial Activations - Best Practice Approach
- Maximizing Research Billing Compliance by Leveraging System Integrations
Refund Policy
Our refund policy is governed by individual products and services refund policy mentioned against each of offerings. However in absence of specific refund policy of an offering below refund policy will be effective.
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. On-Demand Recording purchases will not be refunded as it is available for immediate streaming. However if you are not able to view the webinar or you have any concern about the content of the webinar please contact us at below email or by call mentioning your feedback for resolution of the matter. We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email [email protected] call +1-888-717-2436 (Toll Free).
