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Frequently Asked Questions PDF Print E-mail
  1. Diabetes testing supplies are exempt from CMS accreditation requirements RIGHT?
    • False – Pharmacists selling diabetes testing supplies MUST obtain facility accreditation.

  2. The Medicare Improvements for Patients and Providers Act (MIPPA) of 2008 exempts pharmacists from meeting DMEPOS accreditation requirements?
    • False - MIPPA delayed competitive bidding for 18 to 24 months only. Pharmacists must still obtain facility accreditation to sell DMEPOS, including diabetes supplies.

  3. I don’t have to obtain facility accreditation because diabetes testing supplies aren’t DME like hospitable beds or wheelchairs?
    • False – DMEPOS (Durable Medical Equipment, Prosthetics, Orthotics, and Supplies) INCLUDES diabetes testing supplies. Therefore, you MUST obtain facility accreditation to continue to sell diabetes testing supplies.

  4. Private Insurers (i.e. Blue Cross, HMOs, state Medicaid programs, etc.) do not require DMEPOS accreditation to bill for diabetes testing supplies?
    • False – Many states and private insurers are requiring DMEPOS accreditation to participate in their networks or to collect co-pays from dually-eligible Medicare beneficiaries.

  5. Even though I do not bill Medicare for any diabetes testing supplies, I must still obtain facility accreditation because I bill Medicare for Medicare for Part B drugs and flu shots?
    • False – Pharmacist DO NOT have to obtain DMEPOS accreditation, if they are ONLY billing Medicare for Part B drugs and vaccinations. However, pharmacists MUST update their file with the National Supplier Clearinghouse (NSC) by choosing "Pharmacy" as the supplier type in section 2B, and selecting "Drugs/Pharmaceuticals only" in section 2C of the CMS-855S enrollment form. All other products/services must be removed to assume the accreditation exemption. Failure to update your NSC supplier type may be considered as fraud by CMS.

  6. Where can I acquire current information on Medicare Diabetes Testing Supply Fees?