§ 20-15-2102 — Findings

It is found and determined by the General Assembly of the State of Arkansas that: (1) The process of approval for investigational drugs, biological products, and devices in the United States often takes many years; (2) Patients who have a terminal disease do not have the luxury of waiting until an investigational drug, biological product, or device receives final approval; (3) The standards of the United States Food and Drug Administration for the use of investigational drugs, biological products, and devices may deny the benefits of potentially life-saving treatments to terminally ill patients; (4) The State of Arkansas recognizes that patients who have a terminal disease have a fundamental right to attempt to pursue the preservation of their own lives by accessing available investigational drugs, biological products, and devices; and (5) The use of available investigational drugs, biological products, or devices is a decision that should be made by the patient with a terminal disease in consultation with his or her physician.

Legislative History

Added by Act 2015, No. 374,§ 1, eff. 7/22/2015.