For purposes of this article, unless the context otherwise requires, the following definitions shall apply: (a) âConsulting physicianâ means a physician and surgeon licensed under the Medical Practice Act or an osteopathic physician and surgeon licensed under the Osteopathic Act who performs all of the following: (1) Examines the qualified individual and his or her relevant medical records. (2) Confirms, in writing, the primary physicianâs diagnosis and prognosis. (3) Verifies, in the opinion of the consulting physician, that the eligible patient is competent, acting voluntarily, and has made an informed decision. (b) âEligible patientâ means a person who meets all of the following conditions: (1) Has an immediately life-threatening disease or condition. (2) Has considered all other treatment options currently approved by the United States Food and Drug Administration. (3) Has not been accepted to participate in the nearest clinical trial to his or her home for the immediately life-threatening disease or condition identified in paragraph (1) within one week of completion of the clinical trial application process, or, in the treating physicianâs medical judgment, it is unreasonable for the patient to participate in that clinical trial due to the patientâs current condition and stage of disease. (4) Has received a recommendation from his or her primary physician and a consulting physician for an investigational drug, biological product, or device. (5) Has given written informed consent for the use of the investigational drug, biological product, or device, or, if he or she lacks the capacity to consent, his or her legally authorized representative has given written informed consent on his or her behalf. (6) Has documentation from his or her primary physician and a consulting physician attesting that the patient has met the requirements of this subdivision. (c) âHealth benefit planâ means a plan or program that provides, arranges, pays for, or reimburses the cost of health benefits. âHealth benefit planâ includes, but is not limited to, a health care service plan contract issued by a health care service plan, as defined in Section 1345, and a policy of health insurance, as defined in Section 106 of the Insurance Code, issued by a health insurer. (d) âImmediately life-threatening disease or conditionâ means a stage of disease in which there is a reasonable likelihood that death will occur within a matter of months. (e) âInvestigational drug, biological product, or deviceâ means a drug, biological product, or device that has successfully completed phase one of a clinical trial approved by the United States Food and Drug Administration, but has not been approved for general use by the United States Food and Drug Administration and remains under investigation in a clinical trial approved by the United States Food and Drug Administration. (f) âPrimary physicianâ means a physician and surgeon licensed under the Medical Practice Act or an osteopathic physician and surgeon licensed under the Osteopathic Act. (g) âState regulatory boardâ means the Medical Board of California or the Osteopathic Medical Board of California. (h) (1) âWritten, informed consentâ means a written document that has been approved by the primary physicianâs institutional review board or an accredited independent institutional review board, is signed by an eligible patient, or his or her legally authorized representative when the patient lacks the capacity to consent, and attested to by the patientâs primary physician and a witness that, at a minimum, does all of the following: (A) Explains the currently approved products and treatments for the immediately life-threatening disease or condition from which the patient suffers. (B) Attests to the fact that the patient, or when the patient lacks the capacity to consent his or her legally authorized representative, concurs with the patientâs primary physician in believing t
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