HB 1986
AN ACT relating to the regulation of abortion, including abortion
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
This Texas bill significantly restricts abortion-inducing drug usage by requiring physicians to follow specific FDA-approved protocols and clinical guidelines when providing such medications. Healthcare providers must examine the patient, document pregnancy details, schedule a mandatory follow-up visit within 14 days, and confirm complete pregnancy termination, with potential legal consequences for non-compliance. The bill repeals several existing provisions related to abortion regulation and establishes strict reporting requirements for abortion complications at medical facilities.
Subject Areas
Bill Text
relating to the regulation of abortion, including abortion complication reporting and the repeal of certain laws prohibiting BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF TEXAS: SECTION 1. Sections 171.006(a) and (b), Health and Safety Code, as added by Chapter 4 (H.B. 13), Acts of the 85th Legislature, 1st Called Session, 2017, are amended to read as follows: (a) In this section, "abortion complication" means any harmful event or adverse outcome with respect to a patient related to an abortion that is performed on the patient and that is diagnosed or treated by a health care practitioner or at a health (5) aspiration or allergic response; (11) an infant born alive after the abortion (b) The reporting requirements of this section apply only (A) performs at an abortion facility an abortion that results in an abortion complication diagnosed or treated by (B) diagnoses or treats at an abortion facility an abortion complication that is the result of an abortion performed by another physician at the facility; or (2) a health care facility that is a hospital, abortion facility, freestanding emergency medical care facility, or health care facility that provides emergency medical care, as SECTION 2. Section 171.061, Health and Safety Code, is amended by adding Subdivision (3) and amending Subdivision (8-a) to (3) "Final printed label" means the informational document approved by the United States Food and Drug Administration for an abortion-inducing drug that: (A) outlines the protocol authorized by that agency and agreed to by the drug company applying for authorization of the drug by that agency; and (B) delineates the manner in which a drug is to be used according to approval by that agency. (8-a) "Provide" means, as used with regard to abortion-inducing drugs, any act of giving, selling, dispensing, administering, or otherwise providing or prescribing an SECTION 3. Section 171.063, Health and Safety Code, is amended by amending Subsections (a), (c), and (e) and adding Subsection (b) to read as follows: (a) A person may not knowingly provide an abortion-inducing drug to a pregnant woman for the purpose of inducing an abortion in the pregnant woman or enabling another person to induce an abortion (1) the person who provides the abortion-inducing drug (2) except as otherwise provided by Subsection (b), the provision of the abortion-inducing drug satisfies the protocol tested and authorized by the United States Food and Drug Administration as outlined in the final printed label of the (b) A person may provide the abortion-inducing drug in the dosage amount prescribed by the clinical management guidelines defined by the American College of Obstetricians and Gynecologists Practice Bulletin as those guidelines existed on January 1, 2013. (c) Before the physician provides an abortion-inducing (1) examine the pregnant woman; and (2) document, in the woman's medical record, the gestational age and intrauterine location of the pregnancy (d) A physician who provides the abortion-inducing drug, or the physician's agent, must schedule a follow-up visit for the woman to occur not later than the 14th day after the administration or use of the abortion-inducing drug. At the follow-up visit, the (1) confirm that the woman's pregnancy is completely (2) assess any continued blood loss. SECTION 4. Section 171.206(b), Health and Safety Code, is (a) This subchapter may not be construed to: (1) authorize the initiation of a cause of action against or the prosecution of a woman on whom an abortion is performed or induced or attempted to be performed or induced in (2) wholly or partly repeal, either expressly or by implication, any other statute that regulates or prohibits (3) restrict a political subdivision from regulating or prohibiting abortion in a manner that is at least as stringent as SECTION 5. Section 171.207(b), Health and Safety Code, is (a) Subsection (a) may not be construed to: (1) legalize the conduct prohibited by this (2) limit in any way or affect the availability of a remedy established by Section 171.208; or (3) limit the enforceability of any other laws that SECTION 6. The following provisions are repealed: (1) Chapter 170A, Health and Safety Code; (2) Section 171.061(2-a), Health and Safety Code; (3) Section 171.063(b-1), Health and Safety Code; (4) Section 171.0631, Health and Safety Code; (5) Section 171.0632, Health and Safety Code; (6) Section 171.065, Health and Safety Code; (7) Section 171.066, Health and Safety Code; and (8) Chapter 6-1/2, Title 71, Revised Statutes. SECTION 7. This Act takes effect September 1, 2025.
Bill Sponsors
Legislators who authored or co-sponsored this bill.
Expert Lobbyists for This Bill
These lobbyists specialize in Abortion and related subject areas.
Brianna M. Menard
Gavin L. Massingill
Luis Saenz
Darlene Brugnoli
Jennifer Shelley Rodriguez
Ky Ash
Nora Del Bosque
Craig Holzheauser
Felix Chevalier
Clayton Pope
Bill History
Bill filed: AN ACT relating to the regulation of abortion, including abortion
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