Us Congress 2025-2026 Regular Session

Us Congress House Bill HB1525 Latest Draft

Bill / Introduced Version Filed 03/17/2025

                            I 
119THCONGRESS 
1
STSESSION H. R. 1525 
To prohibit the use or declaration of a public health emergency with respect 
to abortion, and for other purposes. 
IN THE HOUSE OF REPRESENTATIVES 
FEBRUARY24, 2025 
Mr. H
ERNof Oklahoma (for himself, Mr. ADERHOLT, Mr. FEENSTRA, Mr. 
M
OOLENAAR, Mr. BAIRD, Mr. WEBERof Texas, Mr. WEBSTERof Flor-
ida, Mr. C
RENSHAW, Mr. NEWHOUSE, Mr. GREENof Tennessee, Ms. 
B
OEBERT, Mr. RUTHERFORD, Mr. BOST, Mr. GUEST, Mr. SELF, Mr. 
D
OWNING, Mrs. MILLERof Illinois, Mr. DAVIDSON, Mr. ROSE, Mr. HAR-
RIGAN, and Mr. LAMALFA) introduced the following bill; which was re-
ferred to the Committee on Energy and Commerce 
A BILL 
To prohibit the use or declaration of a public health 
emergency with respect to abortion, and for other purposes. 
Be it enacted by the Senate and House of Representa-1
tives of the United States of America in Congress assembled, 2
SECTION 1. SHORT TITLE. 3
This Act may be cited as the ‘‘Protecting Life from 4
Chemical Abortions Act’’. 5
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SEC. 2. NO DECLARATION OF PUBLIC HEALTH EMERGENCY 1
WITH RESPECT TO ABORTION. 2
(a) P
ROHIBITION.—The Secretary of Health and 3
Human Services shall not use or declare any public health 4
emergency under section 319 or 319F–3 of the Public 5
Health Service Act (42 U.S.C. 247d, 247d–6b) with re-6
spect to abortion. 7
(b) T
ERMINATION OF ANYDECLARATION IN EF-8
FECT.—Any declaration described in subsection (a) that 9
is in effect as of the date of enactment of this Act is here-10
by terminated. 11
SEC. 3. LIMITATIONS ON ABORTION DRUG. 12
(a) I
NGENERAL.—The Secretary of Health and 13
Human Services, the Commissioner of Food and Drugs, 14
or any other official within the Department of Health and 15
Human Services, with respect to the applicable risk eval-16
uation and mitigation strategy under section 505–1 of the 17
Federal Food, Drug, and Cosmetic Act (21 U.S.C. 355– 18
1) relating to abortion drugs— 19
(1) may not exercise enforcement discretion 20
with respect to any requirement under such strategy; 21
and 22
(2) shall, effective on the date of the enactment 23
of this Act, reinstate the requirement under such 24
strategy that abortion drugs be dispensed in only 25
clinics, medical offices, and hospitals by or under the 26
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supervision of a certified health care provider (com-1
monly referred to as the ‘‘in-person dispensing re-2
quirement’’). 3
(b) O
THERLIMITATIONS.—With respect to the appli-4
cable risk evaluation and mitigation strategy under section 5
505–1 of the Federal Food, Drug, and Cosmetic Act (21 6
U.S.C. 355–1) relating to an abortion drug, the Secretary 7
of Health and Human Services, the Commissioner of Food 8
and Drugs, or any other official within the Department 9
of Health and Human Services— 10
(1) may not reduce protections (including by 11
means of any update) in such strategy until every 12
State submits to the abortion surveillance system of 13
the Centers for Disease Control and Prevention the 14
abortion data collected in the aggregate from the 15
States and entered into a standardized worksheet 16
that includes questions on the variables specified in 17
subsection (c); and 18
(2) may not waive the requirement under such 19
strategy that such drugs be dispensed in only clinics, 20
medical offices, and hospitals by or under the super-21
vision of a certified health care provider (commonly 22
referred to as the ‘‘in-person dispensing require-23
ment’’). 24
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(c) MANDATORYVARIABLES.—The mandatory vari-1
ables specified in this subsection shall be treated as man-2
datory questions for purposes of section 1903(bb) of the 3
Social Security Act (42 U.S.C. 1396b(bb)) and shall in-4
clude the following: 5
(1) Maternal age in years. 6
(2) Gestational age in completed weeks at the 7
time of abortion. 8
(3) Maternal race. 9
(4) Maternal ethnicity. 10
(5) Maternal race by ethnicity. 11
(6) The abortion method type. 12
(7) Maternal marital status. 13
(8) Previous pregnancies of the mother, includ-14
ing the number of previous live births, the number 15
of previous induced abortions, and the number of 16
previous spontaneous abortions. 17
(9) Maternal residence (State or county). 18
(10) Whether the child survived the abortion. 19
(11) Congenital anomalies. 20
(d) D
EFINITIONS.—In this section: 21
(1) The term ‘‘abortion’’ means the use or pro-22
vision of any instrument, medicine, drug, or any 23
other substance or device— 24
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(A) to intentionally kill the unborn child of 1
a woman known to be pregnant; or 2
(B) to intentionally terminate the preg-3
nancy of a woman known to be pregnant, with 4
an intention other than— 5
(i) after viability to produce a live 6
birth that, if premature, is medically indi-7
cated, and to preserve the life and health 8
of the child born alive; 9
(ii) to treat an ectopic pregnancy; or 10
(iii) to remove a dead unborn child. 11
(2) The term ‘‘abortion drug’’ means any medi-12
cine, drug, or any other substance or combination of 13
drugs, medicine, or substances used for an abortion. 14
(3) The term ‘‘certified health care provider’’ 15
means a health care provider that has completed a 16
Prescriber Agreement Form pursuant to the ele-17
ments for safe use under the applicable risk evalua-18
tion and mitigation strategy under section 505–1 of 19
the Federal Food, Drug, and Cosmetic Act (21 20
U.S.C. 355–1) relating to abortion drugs, under 21
which the provider agrees to the following: 22
(A) The provider has the following quali-23
fications: 24
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(i) Ability to assess the duration of 1
pregnancy accurately. 2
(ii) Ability to diagnose ectopic preg-3
nancies. 4
(iii) Ability to provide surgical inter-5
vention in cases of incomplete abortion or 6
severe bleeding, or to have made plans to 7
provide such care through others, and abil-8
ity to assure patient access to medical fa-9
cilities equipped to provide blood trans-10
fusions and resuscitation, if necessary. 11
(B) The provider will follow the guidelines 12
for use of mifepristone under the applicable risk 13
evaluation and mitigation strategy under sec-14
tion 505–1 of the Federal Food, Drug, and 15
Cosmetic Act (21 U.S.C. 355–1) relating to 16
abortion drugs. 17
(4) The term ‘‘unborn child’’ means an indi-18
vidual organism of the species homo sapiens, begin-19
ning at fertilization, until the point of being born 20
alive as defined in section 8(b) of title 18, United 21
States Code. 22
Æ 
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