Decoding DMEPOS Quality Standards, Part 1 – Provision of Service

By Kris Ravotti, RRT, RCP, Clinical Compliance Educator

Kris Ravotti serves as a clinical compliance educator for DMEPOS, Sleep, Pharmacy, and Dentistry Accreditation Programs at ACHC. A passionate advocate for survey preparedness, Kris is a regular contributor to ACHC’s knowledge bank of FAQs and articles. She also develops audit tools and other materials to support providers on the path to continuing compliance.

Posted: April 13, 2026

Now that CMS requires annual accreditation surveys to ensure DMEPOS suppliers remain compliant with the DMEPOS Quality Standards, it is more important than ever that suppliers fully understand these requirements and how they apply to their daily operations.

This article is the first in a series that reviews key components of the Quality Standards and ACHC DMEPOS Accreditation requirements to help suppliers better understand their responsibilities and the importance of maintaining continuous compliance.

Meeting service requirements

In this piece, the focus is specific to CMS Quality Standards governing the provision of service. This includes ensuring that equipment/products provided are appropriate and function properly, deliveries are complete and accurate, patient education is thorough, and provider-patient follow-up is effective.

For greater emphasis, bold font is used to highlight components less familiar to many suppliers.

 

Maintain safe, clean, functional equipment and manage inventory

▪ Keep equipment in good working order.

○ Maintain a cleaning/disinfection process.

>> Ensure cleaning/disinfection is documented.

>> Ensure equipment is disinfected, safe, and in proper working order before re-issue.

○ Have maintenance/repair procedures.

>> Use and maintain a plan for identifying, monitoring, and reporting equipment and item failure, repair, and preventive maintenance.

>> Ensure all failures, repairs, and preventative maintenance are documented.

○ The maintenance plan should cover all inventory, including discontinued and obsolete, or product that is not patient ready.

▪ Properly store and handle inventory.

○ Separate clean and dirty/returned items, items needing repair, and items that are discontinued or obsolete.

○ Log refrigerated equipment calibration and temperature checks.

○ Identify product recalls and document rapid response.

>> Maintain a tracking system for all patient supplies and equipment by model, serial, or other identifying number that facilitates tracking recalled product locations and identifies theft.

Verify, authenticate, and document before delivering products to an end user that:

>> The product isn’t compromised, damaged, counterfeit, suspected counterfeit, or acquired by fraud or deceit.

>> The product isn’t misbranded and is appropriately labeled for its intended distribution channels.

 

Ensure complete and accurate delivery

▪ Provide information about expected delivery time frames for items and meet them.

○ Deliver and set up all equipment and items within the time frame agreed to by the patient, caregiver, supplier, and prescribing practitioner or coordinate set-up with another supplier.

○ Deliver the scheduled equipment/items on time and ensure equipment delivery personnel are knowledgeable about the equipment/items provided.

Ensure the correct item goes to the correct patient.

○ Match all patient equipment and items delivered to the prescribing practitioner’s order and maintain awareness of identified patient needs, risks, and limitations.

▪ Ensure delivery is complete and documented.

▪ Deliver all necessary equipment, items, or adjustments.

○ Make further applicable adjustments.

During a repair period, deliver or arrange for loaner equipment equal to the original equipment (except for orthotics and prosthetics).

 

Educate patients and caregivers

▪ Patient and caregiver training must fit with equipment and item risks, complexity, and manufacturer instructions and specifications. Suppliers must change training and instructional materials and approaches according to patient and caregiver needs, abilities, learning preferences, and language.

▪ Provide clear (written, pictorial, or verbal) instructions about equipment setup, product features, proper use of product(s)/items, cleaning/maintenance, infection control practices, safety precautions, troubleshooting, and potential hazards of equipment or items, as appropriate.

○ Include written equipment/item instructions. Change instructions according to patient and caregiver abilities, needs, learning preferences, and primary language.

○ Document that you delivered the instructions and that the patient and caregiver understood them. Ensure patients and caregivers know how to safely use the equipment/items.

▪ For initial equipment or items delivered by mail order: Document in the patient record that patient and caregiver training and written instructions on how to use the equipment and items were provided. Include the date, time, and signature of the person providing the services.

Ensure that patients and caregivers can use all equipment and items safely and effectively in their anticipated settings.

▪ Provide information and phone numbers for customer service, regular business hours, after-hours access, equipment or item repair, and emergency coverage.

○ Patients must be able to contact their supplier 24 hours a day, 7 days a week.

 

Provide follow-up care

▪ Suppliers must offer patient and caregiver follow-up services consistent with the equipment, items, and services provided and with prescribing practitioner or other healthcare team member recommendations.

 

Use subcontractors correctly

▪ Have written agreements with all subcontractors.

▪ Ensure that they follow the Quality Standards.

Perform contractor performance evaluations.

Document contractor compliance and accreditation for contractual relationships.

○ Verify that all employees and contractors can participate in federal healthcare programs via the SAM website.

Discover more articles about DMEPOS Accreditation here.