Maximizing Research Billing Compliance by Leveraging System Integrations

Research Billing is complex and often manual process for many health systems. Attendees will learn how system integrations can improve the quality of a health care system’s compliance program

$999.00
Introducing
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Recorded Version Only

(PPT + Recorded Streaming Link)

$349.00
1x Person - Unlimited viewing for 6 Months (For multiple locations contact Customer Care)
rec Recorded Link and Ref. material will be available in My Account Section
Last Recorded Date: May-2021

CD or USB Drive Only

(PPT + Recorded Training File)

$449.00
One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days
Customer Care

Fax: +1-650-362-2367

Email: customercare@fdatrainingalert.com

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Why Should You Attend:

Health systems strive to create a strong and compliant research billing program. This course will help professional understand how technology can play a key role in creating this program.

Many health systems struggle to understand and operationalize the federal regulations supporting research billing. This course will provide insight into building a compliant research billing program and how integrations between a health system’s clinical trials management system (CTMS) and an electronic health record (EHR) will improve their compliance confidence rates. Attendees will learn best practice approaches to creating a research billing program and best practice techniques leveraging technology.

Areas Covered in the Webinar:
  • Various approaches to research billing integrations
  • Compliance with regulations
  • Integration with CTMS and EHR
  • Best practice approaches to creating a compliant program
  • Key challenges facing health systems
  • Effective reporting methods
  • Understand how to build a compliant program
  • Gathering KPIs and metrics to support the research billing program
Who Will Benefit:
  • Clinical Research Coordinators
  • Study Coordinators
  • Clinical Research Finance Analyst
  • Coverage Analysts
  • Research Nurses
  • Administrative Protocol Managers
Free Materials:
  • Reference documents
  • Rule documents or guidance
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.

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. FDATrainingAlert 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.

If you have any concern about the content of the webinar and not satisfied 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 customercare@fdatrainingalert.com call +1-888-771-6965 (Toll Free).

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