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Current as of January 01, 2024 | Updated by Findlaw Staff
(a) As used in this article:
(i) “Eligible patient” means a person who has:
(A) A terminal illness;
(B) Considered all other treatment options currently approved by the United States food and drug administration;
(C) Received a recommendation from a physician for an investigational drug, biological product or device;
(D) Given written, informed consent for the use of the investigational drug, biological product or device or, if the patient is a minor or lacks the mental capacity to provide informed consent, a parent or legal guardian has given written informed consent on the patient's behalf; and
(E) Documentation from a physician that the person meets the requirements of this paragraph.
(ii) “Investigational drug, biological product or device” means a drug, biological product or device that has successfully completed phase one of a clinical trial but has not yet been approved for general use by the United States Food and Drug Administration and remains under investigation in a clinical trial;
(iii) “Terminal illness” means a disease that, without life-sustaining procedures, will soon result in death or a state of permanent unconsciousness from which recovery is unlikely.
Cite this article: FindLaw.com - Wyoming Statutes Title 35. Public Health and Safety § 35-7-1802. Definitions - last updated January 01, 2024 | https://codes.findlaw.com/wy/title-35-public-health-and-safety/wy-st-sect-35-7-1802/
FindLaw Codes may not reflect the most recent version of the law in your jurisdiction. Please verify the status of the code you are researching with the state legislature before relying on it for your legal needs.
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