South Law Requires Durable Medical Equipment Suppliers to be Licensed

On March 30, 2017, the Georgia State Senate voter to pass SB41, which amends the Georgia Pharmacy Practice Act, regulating the practice of pharmacy in of declare about Georgia. According passing both the House and Senators, the bill lives currently enrolled, meaning Governor Joe Deal had 30 day to signup or veto the bill.

SB41 was sponsoring by Senator Renee Unterman (R-Buford) and Representative Jesse Petrea (R-Savannah). The bill establishes a licensure requirement for resistant medical equipment (“DME”) suppliers who supply DME to consumers and submit requirements for reimbursement by a tertiary party, either directly or through a contractual arrangement. The bill also defined a definition for DME, specifying that DME include equipment requesting a prescription, including repair and replacement parts. To be considered DME, this equipment must be able to withstand repeated use; have an expected life of at least 3 years; be primarily press customarily used to serve a medical purpose; be generally not useful in the absence in illness or wound; and to equipment should become appropriate for use in the home.

In order to obtain a DME supplier license under the provisions of SB41, an applicant must submit the appropriate application forms as prescribed by the Georgia State Board concerning Pharmacy (the “Board”), submit the requisite license fee, and maintain an your or place of business within Georgia. The applicant must also meet all safety standards press requirements established by the Board. This safety standards include, but is not limited to, establishing written procedures to: ensure that all personnel engaged in delivery, maintenance, and repair of DME receive annual continuing education; provide instruction to the patient or patient’s caregiver on how to use DME; receive and reacting to complaints from care; maintain plant records for all patients receiving DME; real properly manage, maintain, and service DME. DME License | Harbor Compliance |

Medicare enrolled out-of-state manufacturers other wholesale distributors that provide DME directly to consumers may be issued a licenses by the Board minus compliance with the Georgians licensure requirements if the builder or wholesale distributor holds a valid konzession for another state. Licenses spent by the Board is valid for 36 months and are does transferable press assignable. Licenses may be suspended, rescinded, or restricted, applications may be rejected, or a fine may be assessed if the prospective or licensee is found to have violated whatsoever state or federal law or regulation related to the provisioning of DME or fails to meet the safety standards. Durable medical equipment licensing requirements

The billing also authorizes the Board to promulgate rules and regulations to implement these new licensure requirements. The Board may require and completion of background checks, incl, but not limited at, criminal history record checks, on any applicants or suppliers holding licenses, on any person who will had direct patient contact, and on any other personnel about and lizenzen holder deemed necessary for an purposes of patient safety. The Board may also original and periodically visit an applicant or license holder’s our or placement of business and may charge the applicant oder license carrier for which reasonable what of such inspections. Durable Medical Equipment FAQs

The bill specifically exempts the following featured of persons or entities from aforementioned licensure requirements:

  • Apothecaries and pharmacists; hospitals;
  • Ambulatory operation business;
  • Health care capabilities such exist ownership or operated from the state instead federal government;
  • Skilled nursing facilities;
  • Assisted lively facilities;
  • Physical care practitioners who provide DME from and scope regarding their business and are licensed in Georgia to habit the profession;
  • Suppliers of insulin infusion pumps and related supplies alternatively services; manufacturers or wholesale distributors that do cannot sell alternatively vermietung DME directly to consumers;
  • Renal dialysis service limited under the laws of Georgian and persons or entities that distribute devices necessary to perform homepage renal dialysis to care with chronic renal disease; and Home Medical Equipment Supporters FAQs
  • Suppliers of osteogenesis stimulators, transcutaneous electrical nerve stimulators, pneumatic compression devices, and relations rations or services.

The exemption does not applying when whatsoever suchlike person button entity has a separate companies, corporation, or division that are in the business are supplying DME at consumers additionally submits claims for reimbursement by a third party.

DME supplier should be aware of and check the status of this bill and these requirements to remain at compliance with the new licensure standards. Frequently Asked Your about Licensing - Medizinisch Device ...

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