Section 13.09. Facility requirements.

  All facilities at which prescription drugs are stored, warehoused, handled, held, offered, marketed, or displayed shall:

(1)  Be of suitable size and construction to facilitate cleaning, maintenance, and proper operations;

(2)  Have storage areas designed to provide adequate lighting, ventilation, temperature, sanitation, humidity, space, equipment, and security conditions;

(3)  Have a quarantine area for storage of prescription drugs that are outdated, damaged, deteriorated, misbranded, or adulterated, or that are in immediate or sealed secondary containers that have been opened;

(4)  Be maintained in a clean and orderly condition; and

(5)  Be free from infestation by insects, rodents, birds, or vermin of any kind.

History: Cr. Register, July, 1992, No. 439 , eff. 8-1-92; EmR0815 : emerg. am. (intro.) and (3), eff. 6-1-08; CR 08-051 : am. (intro.) and (3) Register November 2008 No. 635 , eff. 12-1-08.