| Action Summary | In compliance with Chapter 221 of the 2016 Acts of the Assembly, the proposed regulations eliminates definitions that are no longer applicable or now set forth in the Code; provides for permits for third-party logistics providers and for registration of nonresident manufacturers with fees and schedules for renewal of such permits or registrations; includes third-party logistics providers in all sections currently applicable to wholesale distributors; includes nonresident manufacturers in requirements for manufacturers; and eliminates Part IV on pedigree requirements and replaces those regulations with reference to the federal requirements for an electronic, interoperable system to identify, trace, and verify prescription drugs as they are distributed. |
| Chapters Affected | Only affects this chapter. |
| Executive Branch Review | This action will go through the normal Executive Branch Review process. |
| RIS Project | Yes [004822] |
| Associated Mandates |
Chapter: 221 (2016)
|
| New Periodic Review | This action will not be used to conduct a new periodic review. |
| Stage ID | Stage Type | Status |
|---|---|---|
| 7717 | Fast-Track | Stage complete. This regulation became effective on 06/29/2017. |
| Name / Title: | Caroline Juran, RPh / Executive Director |
| Address: |
9960 Mayland Drive Suite 300 Richmond, VA 23233-1463 |
| Email Address: | caroline.juran@dhp.virginia.gov |
| Phone: | (804)367-4456 FAX: (804)527-4472 TDD: ()- |