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<dc:title>119 HR 1562 IH: Test Strip Access Act of 2025</dc:title>
<dc:publisher>U.S. House of Representatives</dc:publisher>
<dc:date>2025-02-25</dc:date>
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<dc:language>EN</dc:language>
<dc:rights>Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain.</dc:rights>
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<distribution-code display="yes">I</distribution-code><congress display="yes">119th CONGRESS</congress><session display="yes">1st Session</session><legis-num display="yes">H. R. 1562</legis-num><current-chamber>IN THE HOUSE OF REPRESENTATIVES</current-chamber><action display="yes"><action-date date="20250225">February 25, 2025</action-date><action-desc><sponsor name-id="C001130">Ms. Crockett</sponsor> (for herself and <cosponsor name-id="G000589">Mr. Gooden</cosponsor>) introduced the following bill; which was referred to the <committee-name committee-id="HIF00">Committee on Energy and Commerce</committee-name></action-desc></action><legis-type>A BILL</legis-type><official-title display="yes">To amend the 21st Century Cures Act to expressly authorize the use of certain grants to implement substance use disorder and overdose prevention activities with respect to fentanyl and xylazine test strips.</official-title></form><legis-body id="H3400F7A99EED4CF28D5104692E61ACBA" style="OLC"><section id="HAE864794346C4E40997F1A4834E6D4E0" section-type="section-one"><enum>1.</enum><header>Short title</header><text display-inline="no-display-inline">This Act may be cited as the <quote><short-title>Test Strip Access Act of 2025</short-title></quote>.</text></section><section id="H09CE7A6ADB6143F9B5B1FDDC97FEBB82"><enum>2.</enum><header>Grant program for State and Tribal response to opioid use disorders</header><text display-inline="no-display-inline">Section 1003(b)(4)(A) of the 21st Century Cures Act (42 U.S.C. 290ee–3a(b)(4)(A)) is amended by inserting <quote>or fentanyl or xylazine test strips</quote> after <quote>which may include drugs or devices approved, cleared, or otherwise legally marketed under the Federal Food, Drug, and Cosmetic Act</quote>.</text></section></legis-body></bill> 

