Delivery of medical devised on behalf of a medical equipment supplier
Purpose of legislation
Provides that a permitted manufacturer, wholesale distributor, warehouser, nonresident warehouser, third-party logistics provider, or nonresident third-party logistics provider or registered nonresident manufacturer or nonresident wholesale distributor (the provider) may deliver a Schedule VI prescription device directly to an ultimate user or consumer, provided certain conditions are met.
|Legislation mandating a change||Chap 242 (2018) Chap 241 (2018)|
|VAC chapters to be amended|
|Associated Regulatory Actions||No regulatory action has been filed.|
|Deadline for the regulation to become effective||12/14/2018|