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    <introducedDate>2025-07-21</introducedDate>
    <congress>119</congress>
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    <constitutionalAuthorityStatementText><![CDATA[<pre>[Congressional Record Volume 171, Number 124 (Monday, July 21, 2025)][House][Pages H3527-H3528]From the Congressional Record Online through the Government Publishing Office [<a href="https://www.gpo.gov">www.gpo.gov</a>]By Mr. NEGUSE:H.R. 4570.[[Page H3528]]Congress has the power to enact this legislation pursuantto the following:Article I, Section 8</pre>]]></constitutionalAuthorityStatementText>
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        <title>Interagency Patent Coordination and Improvement Act of 2025</title>
        <congress>119</congress>
        <number>1097</number>
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          <actionDate>2025-04-10</actionDate>
          <text>Placed on Senate Legislative Calendar under General Orders. Calendar No. 41.</text>
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        <text>Referred to the House Committee on the Judiciary.</text>
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        <bioguideId>N000191</bioguideId>
        <fullName>Rep. Neguse, Joe [D-CO-2]</fullName>
        <firstName>Joe</firstName>
        <lastName>Neguse</lastName>
        <party>D</party>
        <state>CO</state>
        <district>2</district>
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    <policyArea>
      <name>Commerce</name>
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      <policyArea>
        <name>Commerce</name>
        <updateDate>2025-09-11T17:07:21Z</updateDate>
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        <text><![CDATA[<p><strong>Interagency Patent Coordination and Improvement Act of 2025</strong></p><p>This bill establishes the Interagency Task Force on Patents to support coordination and communication between the U.S. Patent and Trademark Office (USPTO) and the Food and Drug Administration (FDA) on activities relating to patents for human drugs and biological products.</p><p>The task force's duties shall include sharing information about (1) the processes of each agency, including how each agency evaluates applications (e.g., patent applications at the USPTO and new drug applications at the FDA); and (2) new approvals of patents, human drugs, biological products, and new technologies. The task force must also establish a process that requires (1) the USPTO to request from the FDA information relating to certain patent applications to help patent examiners carry out their duties, (2) the FDA to provide such information to the USPTO, and (3) the USPTO to assist the FDA in its ministerial role of listing patents.</p>]]></text>
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    <title>Interagency Patent Coordination and Improvement Act of 2025</title>
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        <title>Interagency Patent Coordination and Improvement Act of 2025</title>
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        <title>Interagency Patent Coordination and Improvement Act of 2025</title>
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        <title>To amend title 35, United States Code, to establish an interagency task force between the United States Patent and Trademark Office and the Food and Drug Administration for purposes of sharing information and providing technical assistance with respect to patents, and for other purposes.</title>
        <updateDate>2025-07-31T04:33:32Z</updateDate>
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      <actionDate>2025-07-21</actionDate>
      <text>Referred to the House Committee on the Judiciary.</text>
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    <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>
    <dc:contributor>Congressional Research Service, Library of Congress</dc:contributor>
    <dc:description>This file contains bill summaries and statuses for federal legislation. A bill summary describes the most significant provisions of a piece of legislation and details the effects the legislative text may have on current law and federal programs. Bill summaries are authored by the Congressional Research Service (CRS) of the Library of Congress. As stated in Public Law 91-510 (2 USC 166 (d)(6)), one of the duties of CRS is "to prepare summaries and digests of bills and resolutions of a public general nature introduced in the Senate or House of Representatives". For more information, refer to the User Guide that accompanies this file.</dc:description>
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