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<dc:title>117 S3553 IS: Agility in Manufacturing Preparedness Act</dc:title>
<dc:publisher>U.S. Senate</dc:publisher>
<dc:date>2022-02-02</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">II</distribution-code><congress>117th CONGRESS</congress><session>2d Session</session><legis-num>S. 3553</legis-num><current-chamber>IN THE SENATE OF THE UNITED STATES</current-chamber><action><action-date date="20220202">February 2, 2022</action-date><action-desc><sponsor name-id="S350">Mr. Rubio</sponsor> (for himself and <cosponsor name-id="S337">Mr. Coons</cosponsor>) introduced the following bill; which was read twice and referred to the <committee-name committee-id="SSHR00">Committee on Health, Education, Labor, and Pensions</committee-name></action-desc></action><legis-type>A BILL</legis-type><official-title>To review domestic biopharmaceutical manufacturing capabilities in order to improve public health and medical preparedness and response capabilities and domestic biopharmaceutical manufacturing capabilities.</official-title></form><legis-body display-enacting-clause="yes-display-enacting-clause"><section section-type="section-one" id="S1"><enum>1.</enum><header>Short title</header><text display-inline="no-display-inline">This Act may be cited as the <quote><short-title>Agility in Manufacturing Preparedness Act</short-title></quote>.</text></section><section id="idD856C55255AB4421B763E2EF0C1C1DF3"><enum>2.</enum><header>Review of domestic biopharmaceutical manufacturing capabilities</header><subsection id="id149a8f3b1bce4ee9bb38acc3420c26cd"><enum>(a)</enum><header>In general</header><text>The Secretary of Health and Human Services (referred to in this section as the <quote>Secretary</quote>), in cooperation with the Director of the Biomedical Advanced Research and Development Authority, shall seek to enter into an agreement with the National Institute for Innovation in Manufacturing Biopharmaceuticals to perform the services described in subsection (b).</text></subsection><subsection id="idb5819dc3445e4d68b3a6759fb906d7b2"><enum>(b)</enum><header>Review and recommendations</header><text>Under an agreement described in subsection (a) between the Secretary, the Director of the Biomedical Advanced Research and Development Authority, and the National Institute for Innovation in Manufacturing Biopharmaceuticals, the National Institute for Innovation in Manufacturing Biopharmaceuticals shall—</text><paragraph id="id15e8a9e3a0fd4ef380fd2c1bab1ea4b1"><enum>(1)</enum><text>review current domestic biopharmaceutical manufacturing capacity at the Department of Health and Human Services and its adaptability to various threats; </text></paragraph><paragraph id="idb4aa6bb463eb4c2295f064f46f29fd5a"><enum>(2)</enum><text>draft recommendations for developing, demonstrating, deploying, and advancing new domestic biopharmaceutical manufacturing technologies that address gaps identified under paragraph (1) and align Federal technologies with technologies available to the private sector, including through the new BioMAP initiative of the Biomedical Advanced Research and Development Authority; and</text></paragraph><paragraph id="id56d857428af94cdc8800cad1dbaa5f51"><enum>(3)</enum><text>identify other opportunities and priorities to improve the United States public health and medical preparedness and response capabilities and domestic biopharmaceutical manufacturing capabilities. </text></paragraph></subsection></section></legis-body></bill> 

