decisionhealth Newsletters, Answer Books - 2009 Issue 3 (March)
DME Model Compliance Plan / Essentials of OIG's DME model compliance plan
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Article Overview
This article outlines the essential components of OIG’s model compliance plan for durable medical equipment suppliers. It is useful for compliance, billing, and management teams that want a high-level understanding of the program elements OIG expects, including risk-area awareness, reporting processes, oversight structure, training, audits, and corrective action planning.
Why This Topic Matters
Compliance programs for DME suppliers are closely tied to fraud-prevention and oversight expectations. Understanding the structure and focus areas discussed in the article can help organizations assess whether their internal compliance efforts are aligned with the categories emphasized by OIG.
What You Will Learn
- The core elements of an OIG-style DME compliance plan
- How OIG frames risk-area awareness and internal oversight
- The role of reporting channels, training, auditing, and corrective action in a compliance program
- Why compliance structure and documentation matter for DME suppliers
Who Should Read This
- Durable medical equipment suppliers
- Healthcare compliance officers
- Billing and reimbursement staff
- Healthcare administrators
- Internal audit and risk management teams
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