- Resource Types
- Resource Languages
- Institutional Repository
Keep Browsing
WHDL - 00015484
Visit the home page
About Site Language
WHDL is viewable in multiple languages. Use the pull-down menu to select a language to view the site.
I changed my language, but I’m still seeing resources in the other languages?
If a resource or text has not been translated into your selected language, it will appear in the initially added language. We are always looking for help translating these resources. If you can help, contact us!
Cover Image
Description / Abstract
Research sites with medical billing practices are at risk for clinical research billing (CRB) non-compliance under the False Claims Act, and violations have serious ramifications. Centers for Medicare and Medicaid Services (CMS) have rules and guidelines regarding billing and claims processing requirements when submitting claims. Financial toxicity impacts patients seeking healthcare services through unexpected financial burdens, distress, or decreased satisfaction. Best practices around processes to justify and document financial responsibility during the study start-up process and then the capture of charges for study-related items and services exist across the industry but often differ across sites. Clinical research and medical billing combined may increase site and participant risk of financial toxicity and CRB non-compliance.
Download this Resource
Download Free from WHDL
-
Download as a PDF
File Size Small - 540 KB
Keywordsclinical research, clinical research billing, clinical research billing non-compliance, double-billing, false claims act, financial toxicity, financial toxicity risk, financial transparency, patient-centric, prevention, reduction
Degree AwardedDoctor of Business Administration
Awarding InstitutionIndiana Wesleyan University
Supervisor or ChairDr. Marian Carpenter
Peer Reviewed?Yes
Collections With This Resource
DeVoe Scholar-Practitioner Posters
17 Resources
- Business
- English