HB 3455
AN ACT relating to manufacturer disclosure requirements and liability for
89th Regular Session
Jan 14, 2025 - Jun 2, 2025 • Session ended
Awaiting Committee Assignment
Bill filed, pending referral to House committee
Committee
Not yet assigned
Fiscal Note
Not available
What This Bill Does
Requires manufacturers of experimental drugs or devices to provide comprehensive disclosure forms to purchasers, detailing potential adverse health effects and critical information to help consumers make informed decisions. Health care providers and retailers must personally provide these forms and obtain signed informed consent before selling the experimental product. If a consumer experiences harm from an experimental drug or device sold without proper disclosure, they can sue the manufacturer for damages, including compensation for physical and emotional suffering and legal costs.
Subject Areas
Bill Text
relating to manufacturer disclosure requirements and liability for experimental drugs and devices. BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF TEXAS: SECTION 1. Subchapter E, Chapter 431, Health and Safety Code, is amended by adding Section 431.118 to read as follows: Sec. 431.118. EXPERIMENTAL DRUG OR DEVICE DISCLOSURE REQUIREMENTS; LIABILITY. (a) In this section, "experimental drug or device" means a drug or device that: (1) is experimental or investigational; or (2) has been approved by the United States Food and Drug Administration for emergency use. (b) A manufacturer of an experimental drug or device shall provide to a purchaser of the drug or device a disclosure form that provides a consumer all information reasonably necessary for the consumer to make an informed decision on whether to use the drug or device, including possible adverse health effects of the drug or device, in a clear and coherent summary. (c) A purchaser of an experimental drug or device shall provide the disclosure form described by Subsection (b) to a person to whom the purchaser sells the drug or device. A health care provider or retailer providing or selling the drug or device to a (1) shall provide the disclosure form in person to the (2) may provide or sell the drug or device to the consumer only if a person capable of providing informed consent for the ultimate consumer of the drug or device signs the disclosure. (d) A consumer who receives an experimental drug or device in violation of this section may bring an action against the manufacturer of the drug or device for damages arising from an adverse effect of the drug or device. (e) A prevailing claimant in an action brought under (1) compensatory damages, including damages for physical and emotional pain and suffering; (3) reasonable attorney's fees and costs incurred in SECTION 2. Section 431.118, Health and Safety Code, as added by this Act, applies only to a cause of action that accrues on or after the effective date of this Act. SECTION 3. This Act takes effect September 1, 2025.
Expert Lobbyists for This Bill
These lobbyists specialize in Consumer Protection, Safety and related subject areas.
Beverly C. Cornwell
PremiumMichael J. Johnson
Allison Billodeau
Sarah Hicks
Ky Ash
Andria Baum
David H. Cain
Ashley Michelle Juergens
Elizabeth Hadley
Matthew Bentley
Bill History
Bill filed: AN ACT relating to manufacturer disclosure requirements and liability for
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