DME Proof of Delivery Requirements: How to Comply and Avoid CERT Errors
Learn how to comply with Medicare DME Proof of Delivery (POD) requirements. Avoid CERT denials with this detailed guide covering documentation standards, delivery methods, retention rules, and audit best practices.
KNOWLEDGE CENTER
2/27/20265 min read
Durable Medical Equipment (DME) suppliers continue to face increased scrutiny from the Comprehensive Error Rate Testing (CERT) program. One of the most common denial reasons identified by the CERT Task Force is missing or incomplete Proof of Delivery (POD) documentation. These errors result in claim denials, recoupments, extrapolated overpayments, and heightened audit exposure.
If you bill Medicare Part B for DMEPOS (Durable Medical Equipment, Prosthetics, Orthotics, and Supplies), compliance with Proof of Delivery requirements is not optional. Suppliers must maintain compliant documentation for seven (7) years from the date of service, regardless of the delivery method.
This guide provides a structured overview of:
Medicare POD documentation standards
Required elements for each delivery method
Record retention requirements
Common CERT findings
Audit-proofing best practices
Why Proof of Delivery Matters in Medicare Audits
The Medicare Program Integrity Manual (Chapter 4, §4.7.3) establishes clear standards for delivery documentation. Medicare will not pay for items that are not properly documented as delivered to the beneficiary.
If POD documentation is missing, incomplete, illegible, or inconsistent with claim details, the claim will be denied as “insufficient documentation.”
Importantly:
Proof of Delivery must demonstrate the beneficiary actually received the item.
The date of delivery determines the date of service for billing.
Documentation must be available upon request during CERT, UPIC, or DME MAC audits.
Failure to produce POD during an audit is treated the same as if the documentation never existed.
Standard Documentation Requirements for All DME Claims
Before reviewing delivery methods, it is critical to understand that Proof of Delivery is only one component of documentation. All DME claims must also meet the Standard Documentation Requirements, including:
Valid order (Standard Written Order, when applicable)
Medical necessity documentation
Correct coding
Timely filing
Supplier compliance standards
Signature requirements
Proof of Delivery alone does not establish payment eligibility, but without it, payment cannot be sustained.
Required Elements of Proof of Delivery
The specific POD requirements depend on how the item was delivered. Medicare recognizes three primary delivery methods:
Direct Delivery by the Supplier
Delivery via Shipping or Delivery Service
Delivery to a Nursing Facility on Behalf of a Beneficiary
Each method has distinct documentation requirements.
1. Direct Delivery by the Supplier
When the supplier or its employee delivers the DME item directly to the beneficiary, the following elements must be included in the POD record:
Required Elements:
Beneficiary’s name
Delivery address
Detailed description of item delivered
Must match the HCPCS code billed
Can include brand name, model number, or narrative description
Quantity delivered
Date delivered
Beneficiary (or designee) signature
Printed name of person signing (if signature is illegible)
Relationship to beneficiary (if signed by designee)
Key Compliance Considerations:
The delivery date is the date of service.
Signature stamps are not acceptable.
If the beneficiary cannot sign, documentation must clearly identify the authorized representative.
Electronic signatures are acceptable if compliant with Medicare signature guidelines.
A missing signature is one of the most frequent CERT denial triggers.
2. Delivery via Shipping or Delivery Service
When items are shipped using UPS, FedEx, USPS, or another delivery service, additional safeguards apply.
Required Elements:
You must maintain:
A. Shipping Invoice or Packing Slip
Beneficiary’s name
Shipping address
Detailed description of item
Quantity shipped
Date shipped
AND
B. Delivery Confirmation
Tracking number
Delivery confirmation from carrier
Date delivered
Critical Rules:
The date of service is the shipping date, not the delivery confirmation date.
Documentation must clearly link the tracking number to the specific beneficiary and item billed.
Generic shipping logs are insufficient.
A delivery confirmation showing only “Delivered” without beneficiary identification may not meet requirements unless cross-referenced with internal documentation.
Suppliers often fail to retain both pieces of documentation. Maintaining only a tracking report is insufficient.
3. Delivery to Nursing Facilities on Behalf of a Beneficiary
When DME is delivered to a nursing facility or other institution on behalf of the beneficiary, documentation must show:
Beneficiary name
Facility name and address
Detailed item description
Quantity delivered
Date delivered
Signature of facility representative
Printed name and title of individual accepting delivery
Additionally, documentation must support that the item is not included in the facility’s bundled payment under consolidated billing rules.
This area is high-risk for compliance errors due to:
Consolidated billing restrictions
Inadequate documentation of who accepted delivery
Confusion over Part A versus Part B responsibility
Seven-Year Record Retention Requirement
Suppliers must maintain Proof of Delivery documentation for seven years from the date of service, even if:
The claim was paid
The beneficiary is deceased
The supplier no longer services the beneficiary
The product is a one-time supply
Failure to retain documentation can result in extrapolated overpayments if multiple claims are reviewed and similar errors are identified.
Best practice: Maintain electronic backups in a HIPAA-compliant document management system with indexed retrieval capabilities.
Common CERT Errors Related to Proof of Delivery
The CERT Task Force consistently identifies the following issues:
1. Missing Beneficiary Signature
Unsigned delivery tickets are automatically denied.
2. Illegible Documentation
If auditors cannot read the document, it is considered non-existent.
3. Missing Detailed Description
Documentation that states “DME supplies” without identifying the specific item is insufficient.
4. No Link Between Shipping Record and Claim
Tracking numbers not tied to the specific item billed lead to denial.
5. Incorrect Date of Service
Billing date does not match shipping date or delivery date.
6. Inconsistent Quantity
Quantity billed differs from quantity documented as delivered.
Each of these errors is avoidable with structured internal controls.
Audit-Proofing Your DME Operations
To reduce CERT exposure and maintain compliance, suppliers should implement the following strategies:
1. Standardized POD Templates
Develop delivery forms that automatically include all required elements. Avoid generic templates.
2. Pre-Bill Quality Review
Require staff to verify:
Signature present
Date completed
Item matches HCPCS
Quantity correct
Address verified
No claim should be submitted until POD documentation is complete.
3. Electronic Document Management
Scan and index documents by:
Beneficiary name
Date of service
HCPCS code
Claim number
Ensure secure storage for 7 years.
4. Staff Training
Train intake, warehouse, and billing staff on:
Signature requirements
Shipping documentation rules
Date of service rules
CERT audit response procedures
Compliance is an operational function, not just a billing responsibility.
5. Internal Mock Audits
Conduct quarterly internal reviews:
Randomly select 10–20 claims
Pull full documentation
Verify POD compliance
Document findings
Implement corrective actions
This proactive approach significantly reduces risk.
Relationship Between POD and Medical Necessity
Proof of Delivery confirms the item was delivered. It does not prove the item was medically necessary.
For a claim to withstand audit:
The item must be medically necessary.
A valid order must exist.
All signature requirements must be met.
Proof of Delivery must confirm receipt.
All four components must align.
CERT and DME MAC Oversight
The CERT program estimates improper payment rates nationwide. DME suppliers historically experience higher improper payment rates compared to other provider types due to documentation deficiencies.
CERT findings may trigger:
Focused medical review
Targeted Probe and Educate (TPE)
Prepayment review
Post-payment audit
Referral to Unified Program Integrity Contractors (UPIC)
Consistent POD errors may elevate a supplier’s risk profile.
Risk Management Considerations
From a compliance standpoint, DME suppliers should treat Proof of Delivery as a financial risk control mechanism.
Improper documentation can result in:
Overpayment recoupments
Extrapolated penalties
Civil monetary penalties (in severe cases)
Revocation risk under supplier standards
Reputational damage
Maintaining compliant POD documentation is a core element of Medicare compliance infrastructure.
Practical Compliance Checklist
Use this operational checklist to reduce risk:
✔ Delivery method clearly identified
✔ Detailed item description matches HCPCS code
✔ Quantity documented
✔ Date documented
✔ Valid signature obtained
✔ Relationship documented if not beneficiary
✔ Shipping documentation retained if applicable
✔ Documentation stored for 7 years
✔ Documentation retrievable within 48 hours
If any of these elements are missing, the claim is vulnerable.
References:
Medicare Program Integrity Manual, Chapter 4:
https://www.cms.gov/regulations-and-guidance/guidance/manuals/downloads/pim83c04.pdf
Standard Documentation Requirements for All Claims Submitted to DME MACs:
https://www.cms.gov/medicare-coverage-database/view/article.aspx?articleid=55426
CERT Program Overview:
https://www.cms.gov/research-statistics-data-and-systems/monitoring-programs/medicare-ffs-compliance-programs/cert
Medicare Learning Network® (MLN):
https://www.cms.gov/outreach-and-education/medicare-learning-network-mln

Some or all of the services described herein may not be permissible for HealthBridge US clients and their affiliates or related entities.
The information provided is general in nature and is not intended to address the specific circumstances of any individual or entity. While we strive to offer accurate and timely information, we cannot guarantee that such information remains accurate after it is received or that it will continue to be accurate over time. Anyone seeking to act on such information should first seek professional advice tailored to their specific situation. HealthBridge US does not offer legal services.
HealthBridge US is not affiliated with any department of public health agencies in any state, nor with the Centers for Medicare & Medicaid Services (CMS). We offer healthcare consulting services exclusively and are an independent consulting firm not affiliated with any regulatory organizations, including but not limited to the Accrediting Organizations, the Centers for Medicare & Medicaid Services (CMS), and state departments. HealthBridge is an anti-fraud company in full compliance with all applicable federal and state regulations for CMS, as well as other relevant business and healthcare laws.
© 2026 HealthBridge US, a California corporation. All rights reserved.
For more information about the structure of HealthBridge, visit www.myhbconsulting.com/governance
Legal
Resources
Based in Los Angeles, California, operating in all 50 states.




