HB 3455

AN ACT relating to manufacturer disclosure requirements and liability for

House Bill Shofner
Filed

Filed

Bill introduced by legislator

Committee

Hearing

Passed Cmte

Calendar

Passed

Sent

Enrolled

Governor

Signed

89th Regular Session

Jan 14, 2025 - Jun 2, 2025 • Session ended

Awaiting Committee Assignment

Bill filed, pending referral to House committee

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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.

Bill History

filed

Bill filed: AN ACT relating to manufacturer disclosure requirements and liability for