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Ingested titles 12–51 and 54 from OLRC USLM XML @119-100 (the whole Code now, uniform edition; Title 53 is reserved/empty). LegalText 11,221 -> 59,740; repo total 105,704 records. Deterministic (byte-identical rerun, verified on Title 42's 8,356 sections); make check green. make legal-us-code default now covers every title. Co-Authored-By: Claude Opus 4.8 <noreply@anthropic.com>
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| LegalText | 42 U.S.C. § 285l–5 | Application | us | united_states_code | code_section | 42 | THE PUBLIC HEALTH AND WELFARE | 6A | PUBLIC HEALTH SERVICE | 285l–5 | 42 U.S.C. § 285l–5 | current | 119-100 | 2026-06-26 | official | https://uscode.house.gov/download/releasepoints/us/pl/119/100/xml_usc42@119-100.zip | /us/usc/t42/s285l–5 | data/legal/raw/us/code/title-42/usc42.xml | 6796e73fba15e3ace53482e1dce8b5c49beb0bd72a5ef4082699f6b44723ac78 | 644321055a08eb1f260a6a3e31ac157fa024756abf612a9fd6857e7e400cf24e | 9dded1bcfea90103d6fc86d0051aa6eeffa9e3c4e0e077148b38ec329494ad73 | 2026-07-04 | official |
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42 U.S.C. § 285l–5 - Application
Text
(a) Application Sections 285l–2 to 285l–5 of this title shall not apply to research, including research performed using biotechnology techniques, or research related to the causes, diagnosis, treatment, control, or prevention of physical or mental diseases or impairments of humans or animals.
(b) Use of test methods Nothing in sections 285l–2 to 285l–5 of this title shall prevent a Federal agency from retaining final authority for incorporating the test methods recommended by the ICCVAM in the manner determined to be appropriate by such Federal agency or regulatory body.
(c) Limitation Nothing in sections 285l–2 to 285l–5 of this title shall be construed to require a manufacturer that is currently not required to perform animal testing to perform such tests. Nothing in sections 285l–2 to 285l–5 of this title shall be construed to require a manufacturer to perform redundant endpoint specific testing.
(d) Submission of tests and data Nothing in sections 285l–2 to 285l–5 of this title precludes a party from submitting a test method or scientific data directly to a Federal agency for use in a regulatory program.
(Pub. L. 106–545, § 5, Dec. 19, 2000, 114 Stat. 2724.)
Notes
Editorial Notes
Codification Section was enacted as part of the ICCVAM Authorization Act of 2000, and not as part of the Public Health Service Act which comprises this chapter.