Georgia § 31-52-3 Definitions

Georgia Statutes

§ 31-52-3 — Definitions

Georgia § 31-52-3

Title31

This text of Georgia § 31-52-3 (Definitions) is published on Counsel Stack Legal Research, covering Georgia primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook

O.C.G.A. § 31-52-3 (2026).

Text

As used in this chapter, the term:

(1)"Eligible patient" means a person who meets the requirements of Code Section 31-52-4 .

(2)"Investigational drug, biological product, or device" means a drug, biological product, or device which has successfully completed Phase I of a federal Food and Drug Administration approved clinical trial but has not yet been approved for general use by the federal Food and Drug Administration and currently remains under investigation in a federal Food and Drug Administration approved clinical trial.

(3)"Physician" means a person licensed to practice medicine pursuant to Article 2 of Chapter 34 of Title 43.

(4)"Terminal illness" means a disease that, without life-sustaining procedures, will result in death in the near future and is not considered by a treating

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As used in this chapter, the term: (1) "Eligible patient" means a person who meets the requirements of Code Section 31-52-4 . (2) "Investigational drug, biological product, or device" means a drug, biological product, or device which has successfully completed Phase I of a federal Food and Drug Administration approved clinical trial but has not yet been approved for general use by the federal Food and Drug Administration and currently remains under investigation in a federal Food and Drug Administration approved clinical trial. (3) "Physician" means a person licensed to practice medicine pursuant to Article 2 of Chapter 34 of Title 43. (4) "Terminal illness" means a disease that, without life-sustaining procedures, will result in death in the near future and is not considered by a treating physician to be reversible even with administration of current federal Food and Drug Administration approved and available treatments. (5) "Written informed consent" means a written document that: (A) Is signed by the patient; parent, if the patient is a minor; legal guardian; or health care agent designated by the patient in an advance directive for health care executed pursuant to Chapter 32 of Title 31; (B) Is attested to by the patient's physician and a witness; and (C) Meets the requirements of Code Section 31-52-5 .