Virginia Regulatory Town Hall
Department of Health Professions
Board of Pharmacy
Regulations Governing Wholesale Distributors, Manufacturers and Warehousers [18 VAC 110 ‑ 50]
Delivery of Schedule VI prescription devices
Action 5084
General Information
Action Summary The Board is promulgating emergency regulations in accordance with provisions of ยง 54.1-3415.1 of the Code of Virginia as amended by Chapter 241 of the 2018 Acts of the Assembly. A new section, 18VAC110-50-55, sets out the requirements for delivery of Schedule VI devices directly to an ultimate user or consumer on behalf of a medical equipment supplier upon a valid order from a prescriber or upon request from the medical director of home health agency, nursing home, assisted living facility or hospice.
Chapters Affected Only affects this chapter.
Executive Branch Review This action will go through the normal Executive Branch Review process.
RIS Project Yes  [005526]
Associated Mandates Delivery of medical devise on behalf of a medical equipment supplier
New Periodic Review This action will not be used to conduct a new periodic review.
Stages associated with this regulatory action.
Stage ID Stage Type Status
8333 Emergency/NOIRA Stage complete. Emergency regulation superseded by final permanent regulation.
8584 Proposed Stage complete. Comment period ended 12/13/2019.
8950 Final Stage complete. This regulation became effective on 03/03/2021.
Contact Information
Name / Title: Caroline Juran, RPh  / Executive Director
Address: 9960 Mayland Drive
Suite 300
Richmond, VA 23233-1463
Email Address:
Phone: (804)367-4456    FAX: (804)527-4472    TDD: ()-

This person is the primary contact for this chapter.