I
118THCONGRESS
1
STSESSION H. R. 383
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
JANUARY17, 2023
Mrs. H
ARSHBARGER(for herself, Mr. HERN, Mr. LAMBORN, Mr. BAIRD, Mr.
C
ARTERof Georgia, Mr. WEBERof Texas, Mrs. MILLERof Illinois, Mr.
B
ANKS, Mr. JACKSONof Texas, Mr. WEBSTERof Florida, Mr. DUNCAN,
Mr. F
EENSTRA, Mr. SMITHof New Jersey, and Mr. GOSAR) introduced
the following bill; which was referred to the Committee 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 383 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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