I
119THCONGRESS
1
STSESSION H. R. 679
To nullify the modifications made by the Food and Drug Administration
in January 2023 to the risk evaluation and mitigation strategy for
the abortion pill mifepristone, and for other purposes.
IN THE HOUSE OF REPRESENTATIVES
JANUARY23, 2025
Mrs. H
ARSHBARGER(for herself, Mr. HERNof Oklahoma, Mr. BOST, Mrs.
M
ILLERof Illinois, Mr. WEBERof Texas, Mr. BABIN, Mr. MOOLENAAR,
Mr. W
EBSTERof Florida, Mr. BAIRD, Mr. HIGGINSof Louisiana, Mr.
F
EENSTRA, Mr. YAKYM, Mr. BIGGSof Arizona, Mr. PALMER, and Mr.
G
UEST) introduced the following bill; which was referred to the Com-
mittee on Energy and Commerce
A BILL
To nullify the modifications made by the Food and Drug
Administration in January 2023 to the risk evaluation
and mitigation strategy for the abortion pill mifepristone,
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. NULLIFICATION OF MODIFICATIONS TO REMS 3
FOR MIFEPRISTONE. 4
(a) N
ULLIFICATION.—The modifications made by the 5
Food and Drug Administration in January 2023 to the 6
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•HR 679 IH
risk evaluation and mitigation strategy under section 505– 1
1 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 2
355–1) for mifepristone are hereby nullified. 3
(b) N
OSUBSTANTIALLYSIMILARPROVISIONS.—The 4
Secretary of Health and Human Services (or any head of 5
any office, department, or agency of the Department of 6
Health and Human Services) shall not establish, imple-7
ment, or enforce any provision of a risk evaluation and 8
mitigation strategy under section 505–1 of the Federal 9
Food, Drug, and Cosmetic Act (21 U.S.C. 355–1) for 10
mifepristone that is substantially similar to any of the 11
modifications nullified by subsection (a). 12
Æ
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