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2020 Kentucky Revised Statutes
Chapter 217 - Foods, drugs, and poisons
217.5401 Definitions for KRS 217.5401 to 217.5408.

Universal Citation: KY Rev Stat § 217.5401 (2020)
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217.5401 Definitions for KRS 217.5401 to 217.5408. As used in KRS 217.5401 to 217.5408: (1) "Biological product" means a virus, therapeutic serum, toxin, antitoxin, vaccine, blood, blood component or derivative, protein other than a chemically synthesized polypeptide, allergenic product or analogous product, or arsphenamine or derivative of arsphenamine or any other trivalent organic arsenic compound, applicable to the prevention, treatment, or cure of a disease or condition of human beings; (2) "Device" has the same meaning as in KRS 217.015; (3) "Drug" has the same meaning as in KRS 217.015; (4) "Eligible patient" means an individual who meets the requirements of KRS 217.5403; (5) "Health care provider" means a licensed physician, a licensed advanced practice registered nurse, or a licensed physician assistant; (6) "Health facility" has the same meaning as in KRS 216B.015; (7) "Investigational drug, biological product, or device" means a drug, biological product, or device that: (a) Has successfully completed Phase I of a clinical trial but has not yet been approved for general use by the United States Food and Drug Administration; and (b) Remains under investigation in a United States Food and Drug Administration-approved clinical trial; (8) "Terminal illness" means a progressive disease or a medical or surgical condition that: (a) Entails significant functional impairment; (b) Is not considered by a treating health care provider to be reversible even with administration of a treatment currently approved by the United States Food and Drug Administration; and (c) Without life-sustaining procedures, will result in death; and (9) "Written informed consent" means a written document that meets the requirements of KRS 217.5404. Effective: June 29, 2017 History: Created 2017 Ky. Acts ch. 65, sec. 1, effective June 29, 2017.
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