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<bill bill-stage="Introduced-in-Senate" dms-id="A1" public-private="public" slc-id="S1-TAM21035-FJC-7Y-588"><metadata xmlns:dc="http://purl.org/dc/elements/1.1/">
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<dc:title>117 S373 IS: Better Empowerment Now to Enhance Framework and Improve Treatments Act of 2021</dc:title>
<dc:publisher>U.S. Senate</dc:publisher>
<dc:date>2021-02-23</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>1st Session</session><legis-num>S. 373</legis-num><current-chamber>IN THE SENATE OF THE UNITED STATES</current-chamber><action><action-date date="20210223">February 23, 2021</action-date><action-desc><sponsor name-id="S318">Mr. Wicker</sponsor> (for himself and <cosponsor name-id="S311">Ms. Klobuchar</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 strengthen the use of patient-experience data within the benefit-risk framework for approval of new drugs.</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>Better Empowerment Now to Enhance Framework and Improve Treatments Act of 2021</short-title></quote> or the <quote><short-title>BENEFIT Act of 2021</short-title></quote>.</text></section><section id="idED1EC87955AD4F448A70B22CAA9BBDE9"><enum>2.</enum><header>Strengthening the use of patient-experience data within benefit-risk framework</header><text display-inline="no-display-inline">Section 569C of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/360bbb-8c">21 U.S.C. 360bbb–8c</external-xref>) is amended—</text><paragraph id="idCF23BD1A74C945AA8078FF4F40CAB52A"><enum>(1)</enum><text display-inline="yes-display-inline">in subsection (a)(1)—</text><subparagraph id="idEBC1760BFB724D7F9F7CDBA19EB12299"><enum>(A)</enum><text display-inline="yes-display-inline">in subparagraph (A), by striking <quote>; and</quote> and inserting a semicolon;</text></subparagraph><subparagraph id="id5A0A146C53E744CB9CFCF5D18EDA9C17"><enum>(B)</enum><text>in subparagraph (B), by striking the period and inserting <quote>; and</quote>; and</text></subparagraph><subparagraph id="id07E20FC35C364AE8B57BF08BEB2C1FF1"><enum>(C)</enum><text>by adding at the end the following:</text><quoted-block style="OLC" display-inline="no-display-inline" id="idB3BB204F98034757AF9819D6C35E24E2"><subparagraph id="idF2E3B33AB739455CB2CCC97C6701ADC2"><enum>(C)</enum><text>as part of the risk-benefit assessment framework in the new drug approval process described in section 505(d), considering relevant patient-focused drug development data, such as data from patient preference studies (benefit-risk), patient reported outcome data, or patient experience data, developed by the sponsor of an application or another party.</text></subparagraph><after-quoted-block>; and</after-quoted-block></quoted-block></subparagraph></paragraph><paragraph id="idA9F94823F4E0489AA9C85B20CBCE6CE8"><enum>(2)</enum><text>in subsection (b)(1), by inserting <quote>, including a description of how such data and information were considered in the risk benefit assessment described in section 505(d)</quote> before the period.</text></paragraph></section></legis-body></bill>


