[Congressional Bills 117th Congress]
[From the U.S. Government Publishing Office]
[S. 5002 Engrossed in Senate (ES)]
<DOC>
117th CONGRESS
2d Session
S. 5002
_______________________________________________________________________
AN ACT
To allow for alternatives to animal testing for purposes of drug and
biological product applications.
Be it enacted by the Senate and House of Representatives of the
United States of America in Congress assembled,
SECTION 1. SHORT TITLE.
This Act may be cited as the ``FDA Modernization Act 2.0''.
SEC. 2. ALTERNATIVES TO ANIMAL TESTING.
(a) In General.--Section 505 of the Federal Food, Drug, and
Cosmetic Act (21 U.S.C. 355) is amended--
(1) in subsection (i)--
(A) in paragraph (1)(A), by striking ``preclinical
tests (including tests on animals)'' and inserting
``nonclinical tests''; and
(B) in paragraph (2)(B), by striking ``animal'' and
inserting ``nonclinical tests''; and
(2) after subsection (y), by inserting the following:
``(z) Nonclinical Test Defined.--For purposes of this section, the
term `nonclinical test' means a test conducted in vitro, in silico, or
in chemico, or a non-human in vivo test that occurs before or during
the clinical trial phase of the investigation of the safety and
effectiveness of a drug, and may include animal tests, or non-animal or
human biology-based test methods, such as cell-based assays,
microphysiological systems, or bioprinted or computer models.''.
(b) Biosimilar Biological Product Applications.--Item (bb) of
section 351(k)(2)(A)(i)(I) of the Public Health Service Act (42 U.S.C.
262(k)(2)(A)(i)(I)) is amended to read as follows:
``(bb) an assessment of
toxicity (which may rely on, or
consist of, a study or studies
described in item (aa) or
(cc)); and''.
Passed the Senate September 29, 2022.
Attest:
Secretary.
117th CONGRESS
2d Session
S. 5002
_______________________________________________________________________
AN ACT
To allow for alternatives to animal testing for purposes of drug and
biological product applications.