119-s1830

S
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Right to Treat Act

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Introduced:
May 21, 2025
Policy Area:
Health

Bill Statistics

2
Actions
0
Cosponsors
0
Summaries
1
Subjects
1
Text Versions
Yes
Full Text

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Latest Action

May 21, 2025
Read twice and referred to the Committee on Health, Education, Labor, and Pensions.

Actions (2)

Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
Type: IntroReferral | Source: Senate
May 21, 2025
Introduced in Senate
Type: IntroReferral | Source: Library of Congress | Code: 10000
May 21, 2025

Subjects (1)

Health (Policy Area)

Text Versions (1)

Introduced in Senate

May 21, 2025

Full Bill Text

Length: 1,982 characters Version: Introduced in Senate Version Date: May 21, 2025 Last Updated: Nov 14, 2025 6:19 AM
[Congressional Bills 119th Congress]
[From the U.S. Government Publishing Office]
[S. 1830 Introduced in Senate

(IS) ]

<DOC>

119th CONGRESS
1st Session
S. 1830

To clarify that agencies of the Department of Health and Human Services
do not have the authority to regulate the practice of medicine.

_______________________________________________________________________

IN THE SENATE OF THE UNITED STATES

May 21, 2025

Mr. Johnson introduced the following bill; which was read twice and
referred to the Committee on Health, Education, Labor, and Pensions

_______________________________________________________________________

A BILL

To clarify that agencies of the Department of Health and Human Services
do not have the authority to regulate the practice of medicine.

Be it enacted by the Senate and House of Representatives of the
United States of America in Congress assembled,
SECTION 1.

This Act may be cited as the ``Right to Treat Act''.
SEC. 2.

(a) In General.--Subject to subsection

(b) and notwithstanding any
other provision of law--

(1) no Federal agency, including the Food and Drug
Administration, the National Institutes of Health, and the
Centers for Disease Control and Prevention, shall have the
authority to regulate the practice of medicine; and

(2) no Federal law, rule, regulation, or policy shall
prohibit or restrict the prescription or disbursement for an
unapproved use of any drug that is approved by the Food and
Drug Administration, or that is available pursuant to
section 561B of the Federal Food, Drug, and Cosmetic Act (21 U.
360bbb-0a).

(b) Rule of Construction.--Nothing in this Act shall be construed
to affect any Federal law, rule, regulation, or policy that restricts
abortion, assisted suicide, euthanasia, mercy killing, coercive family
planning, female genital mutilation, or gender transition medical
interventions.
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