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386 chapters · 8,532 sections in this title.
Tex. Health and Safety Code § 489.001 Definitions
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Sec. 489.001. DEFINITIONS. In this chapter: (1) "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 …
Tex. Health and Safety Code § 489.051 Patient Eligibility
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Sec. 489.051. PATIENT ELIGIBILITY. A patient is eligible to access and use an investigational drug, biological product, or device under this chapter if: (1) the patient has a terminal illness, attested to by the patient's treating physician; and (2) the patient's physician: (A) i…
Tex. Health and Safety Code § 489.052 Informed Consent
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Sec. 489.052. INFORMED CONSENT. (a) Before receiving an investigational drug, biological product, or device, an eligible patient must sign a written informed consent. If the patient is a minor or lacks the mental capacity to provide informed consent, a parent or legal guardian ma…
Tex. Health and Safety Code § 489.053 Provision of Investigational Drug, Biological Product, Or Device By Manufacturer
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Sec. 489.053. PROVISION OF INVESTIGATIONAL DRUG, BIOLOGICAL PRODUCT, OR DEVICE BY MANUFACTURER. (a) A manufacturer of an investigational drug, biological product, or device may make available the manufacturer's investigational drug, biological product, or device to eligible patie…