1. (1) A medicare-approved dialysis center, a facility operating a medicare-approved home dialysis program, a manufacturer, or a wholesaler who sells, delivers, possesses, or dispenses dialysis devices and legend drugs directly to its home dialysis patients permitted by RCW 18.64.257 and 69.41.032 shall attach a record of shipment to the practitioner's order. The record of shipment shall include:

   1. (a) The name of the patient;
   2. (b) Strengths and quantities of drugs, if applicable;
   3. (c) Device name, if applicable;
   4. (d) The name of the drug manufacturer, if applicable;
   5. (e) The name of the device manufacturer, if applicable;
   6. (f) Date of shipment;
   7. (g) Names of persons who selected, assembled and packaged for shipment; and
   8. (h) The name of the pharmacist or designated individual responsible for the shipment.
2. (2) Prescription records, and drug and device shipment records shall be maintained in accordance with WAC 246-945-020.

[Statutory Authority: RCW 18.64.005, 18.64.257, and 69.41.032. WSR 25-07-093, s 246-945-092, filed 3/18/25, effective 4/18/25. Statutory Authority: RCW 18.64.005, 18.64.080, 18.130.075, 18.64.043, 18.64.044, 18.64.045, 18.64.046, 18.64.370, 18.64.460, 69.50.310, 18.64.011, 18.64.245, 18.64.470, 18.64.255, 18.64.205, 18.64.253, 18.64.410, 18.64.500, 18.64.590. WSR 20-12-072, § 246-945-092, filed 6/1/20, effective 7/1/20.]