A.R.S. § 32-1980: Virtual manufacturers; oversight and contracting requirements

A. A virtual manufacturer located in this state or located in another jurisdiction that is responsible for the shipment of prescription drugs or devices into this state shall make professionally reasonable efforts to ensure that the United States food and drug administration registered manufacturing entity for the physical manufacture of a prescription drug or prescription device complies with current good manufacturing practices as described in 21 Code of Federal Regulations part 210, 211, 212, 314, 808, 812 or 820, as applicable.

B. A virtual manufacturer of prescription drugs shall contract with a drug manufacturer that is permitted by this state.