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HR 5222 103th Congress House

Consumer Products Safe Testing Act

Official title: To provide for nonanimal acute toxicity testing by the Federal Government.

Introduced: October 6, 1994 See on congress.gov
Animals Administrative procedureCommerceEnvironmental ProtectionEvaluation
More subjectsShow fewer subjects
Government Operations and PoliticsLaboratory animalsProduct safetyProtection of animalsScience, Technology, Communications
This bill died when the 103rd Congress ended
It never became law before the 103rd Congress (1993–1994) adjourned, and bills don't carry over to the next Congress. It would have to be reintroduced. You can still save it for reference, but it won't receive updates.
 Everywhere this bill has been 4 steps
Introduced
In committee
Reported out
Passed House
Passed Senate
To President
Became law
Nov 16, 1994
Referred to the Subcommittee on Commerce, Consumer Protection and Competitiveness.
Oct 8, 1994
Sponsor introductory remarks on measure. (CR E2210)
Oct 6, 1994
Referred to the House Committee on Energy and Commerce.
Oct 6, 1994
Introduced in House
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 Latest action November 16, 1994

Referred to the Subcommittee on Commerce, Consumer Protection and Competitiveness.

 Plain-English summary Congressional Research Service

Consumer Products Safe Testing Act - Requires each Federal department or agency (department) head to: (1) evaluate any regulation, guideline, or recommendation issued by that department which requires, recommends, or encourages the use of the Draize or other animal acute toxicity test (animal test) to evaluate the safety of a regulated product; (2) evaluate nonanimal alternatives with the potential for partial or full replacement of such test; and (3) promulgate regulations, guidelines, or recommendations that specify a nonanimal acute toxicity test or battery of tests that should be used instead of an animal test unless the nonanimal test is less likely to predict the acute health effects of a product on humans.

Directs the appropriate Federal department, if a determination is made that no nonanimal test is as likely to predict the human reaction to the regulated product as the animal test, to publish in the Federal Register an explanation of all options considered and the justification for continuing the animal test, which shall be subject to public comment.

Requires each Federal department head, at least every two years (beginning three years after this Act's enactment date), after considering the most recent technological advances available, to determine whether continued use of any animal test is justified (and if the department head determines that such use is justified, such head shall publish an explanation and justification for such continued use in the Federal Register, which shall be subject to public comment).

Makes this Act inapplicable to regulations, guidelines, or recommendations related to medical research.

 Bill text 1 version

Source documents hosted by congress.gov.

 Committees of jurisdiction 2
Cite this page click to expand
APA
U.S. Congress. (2026). H.R. 5222: Consumer Products Safe Testing Act. 103rd Congress. Open America. https://openamerica.io/bill/103-HR-5222/
MLA
"H.R. 5222: Consumer Products Safe Testing Act." 103rd Congress, 2026, Open America, https://openamerica.io/bill/103-HR-5222/.
Bluebook (legal)
H.R. 5222, 103rd Cong. (2026), https://openamerica.io/bill/103-HR-5222/.
Markdown link
[H.R. 5222: Consumer Products Safe Testing Act](https://openamerica.io/bill/103-HR-5222/)
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