CMS Transitions CLIA to Electronic Fee Coupons and Certificates: What Laboratories Must Do Before March 1, 2026

CMS is transitioning the Clinical Laboratory Improvement Amendments (CLIA) program to electronic fee coupons and certificates effective March 1, 2026. Learn what laboratories must do to avoid billing disruptions and certification issues.

KNOWLEDGE CENTER

2/27/20264 min read

The Centers for Medicare & Medicaid Services (CMS) is implementing a significant modernization of the Clinical Laboratory Improvement Amendments (CLIA) program. Beginning March 1, 2026, CMS will discontinue paper fee coupons and paper CLIA certificates. Laboratories will no longer receive mailed documents, and payment of CLIA certification and survey fees will be required online. Paper checks will no longer be accepted.

This transition is part of CMS’s broader digital transformation efforts aimed at improving administrative efficiency, reducing delays, enhancing communication accuracy, and strengthening regulatory oversight.

Laboratories and providers that perform laboratory testing under a CLIA certificate must act immediately to enroll in electronic notifications and ensure their contact information is up to date. Failure to transition to electronic communication may result in billing issues, delayed certification processing, or compliance risks.

Overview of CLIA and Why This Change Matters

The Clinical Laboratory Improvement Amendments (CLIA) of 1988 establish quality standards for laboratory testing performed on human specimens for health assessment, diagnosis, prevention, or treatment of disease. CMS regulates laboratories under CLIA to ensure accuracy, reliability, and timeliness of test results.

All laboratories performing testing on human specimens must hold a valid CLIA certificate appropriate to the complexity of testing conducted. These include:

  • Certificate of Waiver

  • Certificate of Provider-Performed Microscopy Procedures (PPMP)

  • Certificate of Registration

  • Certificate of Compliance

  • Certificate of Accreditation

Maintaining active CLIA certification requires:

  • Timely payment of certification fees

  • Payment of survey fees (when applicable)

  • Successful completion of inspections or accreditation reviews

  • Ongoing compliance with federal laboratory standards

The shift to electronic fee coupons and certificates directly impacts these administrative and compliance processes.

What Is Changing on March 1, 2026?

Effective March 1, 2026:

  1. CMS will no longer mail paper CLIA fee coupons.

  2. CMS will no longer mail paper CLIA certificates.

  3. Laboratories must pay CLIA certification and survey fees online.

  4. Paper checks will no longer be accepted.

This means that laboratories relying on mailed invoices or physical certificates for compliance documentation will need to update their internal workflows immediately.

CMS has clarified that this is the final opportunity for eligible laboratories and providers to enroll in electronic notifications.

Why CMS Is Eliminating Paper CLIA Documents

The transition reflects CMS’s efforts to:

  • Reduce administrative delays caused by mailing and manual processing

  • Improve billing accuracy and real-time fee tracking

  • Decrease lost or delayed certificates

  • Enhance environmental sustainability

  • Strengthen digital compliance tracking

Paper-based systems have historically created delays in certification renewals and billing reconciliation. Electronic delivery ensures immediate access to required documentation and reduces the risk of lapses in certification due to misplaced mail.

Who Is Affected?

The transition applies to:

  • Independent clinical laboratories

  • Hospital-based laboratories

  • Physician office laboratories (POLs)

  • Home health agencies performing lab testing

  • Hospice agencies performing lab testing

  • Skilled nursing facilities conducting testing

  • Any provider performing laboratory testing under CLIA certification

Important Exception:
This change does not apply to CLIA-exempt states.

CLIA-exempt states operate under state laboratory programs that CMS has determined meet or exceed federal CLIA requirements. Laboratories in those states should verify whether this transition impacts their specific processes.

Risks of Not Switching to Electronic Notifications

Failure to enroll in electronic notifications or update email information may result in:

  • Missed fee coupons

  • Delayed fee payments

  • Lapsed CLIA certification

  • Survey scheduling disruptions

  • Billing discrepancies

  • Compliance violations

From a regulatory standpoint, an expired CLIA certificate can result in immediate operational consequences. Laboratories may not legally perform testing without a valid CLIA certificate corresponding to the testing complexity.

In addition, Medicare reimbursement for laboratory services may be impacted if certification lapses occur.

How to Switch to Electronic CLIA Notifications

Laboratories must proactively transition to electronic communication by completing one of the following steps:

Option 1: Contact Your State Agency

Email your state CLIA agency to:

  • Enroll in electronic notifications

  • Confirm your laboratory’s email address

  • Update contact information

Each state maintains a designated CLIA contact. Laboratories should ensure the email provided is monitored by compliance or billing personnel.

Option 2: Contact Your Accreditation Organization

If your laboratory holds a Certificate of Accreditation, you must contact your Accreditation Organization (AO), such as:

  • College of American Pathologists (CAP)

  • The Joint Commission

  • COLA

  • AABB

Accredited laboratories should confirm that their AO has the correct email contact on file for CLIA communications.

Internal Compliance Action Plan for Laboratories

To prevent disruption, laboratories should implement the following internal controls:

1. Designate a Responsible Contact

Assign a compliance officer, laboratory director, or billing manager as the primary CLIA contact.

2. Update Contact Information

Ensure that:

  • Email addresses are accurate

  • Generic mailboxes (e.g., compliance@ or billing@) are monitored

  • Spam filters allow CMS communications

3. Revise Billing Procedures

Since paper checks will no longer be accepted:

  • Establish online payment access

  • Coordinate with finance departments

  • Update internal SOPs for fee processing

4. Update Policy and Procedure Manuals

Revise compliance manuals to reflect:

  • Electronic receipt of CLIA certificates

  • Electronic fee management

  • Online payment protocols

5. Maintain Electronic Records

Develop secure storage for:

  • Electronic CLIA certificates

  • Payment confirmations

  • Fee coupon documentation

These records may be required during inspections or audits.

Implications for Multi-Site and Corporate Laboratory Entities

Organizations operating multiple laboratory sites must ensure:

  • Each CLIA number is properly enrolled

  • Each location has accurate contact information

  • Corporate compliance teams coordinate with site-level leadership

Failure to enroll all sites may result in partial billing failures or certification discrepancies.

Corporate healthcare organizations, including home health and hospice providers operating under multiple CLIA certificates, should conduct a full inventory review of all active CLIA numbers.

Impact on Survey and Inspection Scheduling

CLIA certification cycles typically run every two years. Laboratories receive fee coupons before the certificate expiration date.

If electronic enrollment is incomplete:

  • Survey scheduling may be delayed

  • Certification renewal may not process timely

  • Risk of temporary suspension increases

Timely electronic enrollment ensures seamless survey coordination and uninterrupted certification cycles.

Financial and Regulatory Considerations

From a regulatory compliance perspective, laboratories must view this change as a mandatory modernization requirement, not an optional administrative update.

Key financial considerations include:

  • Ensuring timely online payments to avoid penalties

  • Reconciling electronic invoices with internal accounting systems

  • Budgeting for potential IT updates

Noncompliance could expose laboratories to:

  • Civil monetary penalties

  • Suspension of testing

  • Loss of Medicare billing privileges

Best Practices for Compliance Leaders

Compliance officers and laboratory directors should:

  • Conduct immediate readiness assessments

  • Communicate changes to executive leadership

  • Train administrative and billing teams

  • Audit CLIA certificate expiration dates

  • Document all communication with CMS or AOs

Proactive compliance management reduces regulatory risk and operational disruption.

Timeline Summary

Now – February 29, 2026
Laboratories must enroll in electronic notifications and update contact information.

March 1, 2026
Paper fee coupons and certificates are discontinued. Online payments required. Paper checks are no longer accepted.

After March 1, 2026
Laboratories not enrolled may experience billing or certification issues.

Strategic Considerations for Healthcare Organizations

For healthcare systems and compliance-driven organizations, this transition presents an opportunity to:

  • Centralize regulatory documentation

  • Digitize compliance workflows

  • Strengthen audit preparedness

  • Reduce reliance on manual processes

Organizations that integrate CLIA tracking into broader compliance dashboards will gain operational efficiencies.

Final Takeaway

CMS’s transition to electronic CLIA fee coupons and certificates represents a mandatory modernization effort that directly affects every laboratory operating under CLIA certification, except those in exempt states.

The deadline of March 1, 2026 is firm. Laboratories must:

  • Enroll in electronic notifications

  • Update email contact information

  • Prepare for mandatory online fee payment

  • Eliminate reliance on paper checks and mailed certificates

Failure to act may result in certification lapses, billing complications, and regulatory risk.

Compliance leaders should treat this change as an urgent administrative priority to ensure uninterrupted laboratory operations.

Official Resources

CMS CLIA Program Overview:
https://www.cms.gov/Regulations-and-Guidance/Legislation/CLIA

State Agency Contact Information (CLIA):
https://www.cms.gov/Regulations-and-Guidance/Legislation/CLIA/Downloads/CLIASA.pdf

Accreditation Organizations Approved by CMS:
https://www.cms.gov/Regulations-and-Guidance/Legislation/CLIA/Downloads/AOList.pdf