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    <introducedDate>2008-06-12</introducedDate>
    <congress>110</congress>
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      <item>
        <title>Access, Compassion, Care, and Ethics for Seriously Ill Patients Act</title>
        <congress>110</congress>
        <number>3046</number>
        <type>S</type>
        <latestAction>
          <actionDate>2008-05-21</actionDate>
          <text>Read twice and referred to the Committee on Health, Education, Labor, and Pensions.</text>
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        <text>Referred to the Subcommittee on Health.</text>
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        <actionDate>2008-06-12</actionDate>
        <text>Referred to the Committee on Energy and Commerce, and in addition to the Committee on Ways and Means, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.</text>
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        <text>Referred to the Committee on Energy and Commerce, and in addition to the Committee on Ways and Means, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.</text>
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        <text>Referred to the Committee on Energy and Commerce, and in addition to the Committee on Ways and Means, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.</text>
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        <fullName>Rep. Watson, Diane E. [D-CA-33]</fullName>
        <firstName>Diane</firstName>
        <lastName>Watson</lastName>
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        <state>CA</state>
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        <fullName>Rep. Burton, Dan [R-IN-5]</fullName>
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        <party>R</party>
        <state>IN</state>
        <district>5</district>
        <sponsorshipDate>2008-06-12</sponsorshipDate>
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        <fullName>Rep. Latham, Tom [R-IA-4]</fullName>
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        <party>R</party>
        <state>IA</state>
        <district>4</district>
        <sponsorshipDate>2008-06-12</sponsorshipDate>
        <isOriginalCosponsor>True</isOriginalCosponsor>
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        <fullName>Rep. Johnson, Eddie Bernice [D-TX-30]</fullName>
        <firstName>EDDIE</firstName>
        <lastName>JOHNSON</lastName>
        <party>D</party>
        <state>TX</state>
        <middleName>BERNICE</middleName>
        <district>30</district>
        <sponsorshipDate>2008-06-12</sponsorshipDate>
        <isOriginalCosponsor>True</isOriginalCosponsor>
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        <fullName>Rep. Solis, Hilda L. [D-CA-32]</fullName>
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        <party>D</party>
        <state>CA</state>
        <middleName>L.</middleName>
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        <sponsorshipDate>2008-06-12</sponsorshipDate>
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        <fullName>Rep. Jackson-Lee, Sheila [D-TX-18]</fullName>
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        <lastName>JACKSON-LEE</lastName>
        <party>D</party>
        <state>TX</state>
        <district>18</district>
        <sponsorshipDate>2008-06-12</sponsorshipDate>
        <isOriginalCosponsor>True</isOriginalCosponsor>
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      <item>
        <bioguideId>C000984</bioguideId>
        <fullName>Rep. Cummings, Elijah E. [D-MD-7]</fullName>
        <firstName>ELIJAH</firstName>
        <lastName>CUMMINGS</lastName>
        <party>D</party>
        <state>MD</state>
        <middleName>E.</middleName>
        <district>7</district>
        <sponsorshipDate>2008-06-12</sponsorshipDate>
        <isOriginalCosponsor>True</isOriginalCosponsor>
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        <fullName>Rep. Conyers, John, Jr. [D-MI-14]</fullName>
        <firstName>JOHN</firstName>
        <lastName>CONYERS</lastName>
        <party>D</party>
        <state>MI</state>
        <district>14</district>
        <sponsorshipDate>2008-06-12</sponsorshipDate>
        <isOriginalCosponsor>True</isOriginalCosponsor>
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    <policyArea>
      <name>Health</name>
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    <subjects>
      <legislativeSubjects>
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          <name>Clinical trials</name>
        </item>
        <item>
          <name>Commerce</name>
        </item>
        <item>
          <name>Department of Health and Human Services</name>
        </item>
        <item>
          <name>Drug approvals</name>
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        <item>
          <name>Drug industry</name>
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        <item>
          <name>Drugs</name>
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        <item>
          <name>Executive reorganization</name>
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          <name>Federal advisory bodies</name>
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          <name>Government Operations and Politics</name>
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          <name>Medical supplies</name>
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          <name>Medical technology</name>
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          <name>Medicare</name>
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          <name>Patients' rights</name>
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          <name>Product safety</name>
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        <item>
          <name>Products liability</name>
        </item>
        <item>
          <name>Science, Technology, Communications</name>
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        <item>
          <name>Social Welfare</name>
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        <name>Health</name>
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    <summaries>
      <summary>
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        <actionDate>2008-06-12</actionDate>
        <actionDesc>Introduced in House</actionDesc>
        <updateDate>2008-09-09T22:22:23Z</updateDate>
        <text><![CDATA[ <p>Access, Compassion, Care, and Ethics for Seriously Ill Patients Act or the ACCESS Act - Amends the Federal Food, Drug, and Cosmetic Act to require the Secretary of Health and Human Services to permit an investigational drug, biological product, or device to be made available for expanded access under a treatment investigational new drug application or treatment investigational device exemption if specified Compassionate Investigational Access requirements are met.</p><p>Gives immunity to the manufacturer, distributor, administrator, sponsor, or physician from suit or liability relating to products approved under this Act. </p><p>Establishes a procedure for accelerated approval of an investigational drug, biological product, or device that is reasonably likely to predict clinical benefit to a patient suffering from a serious or life-threatening condition.</p><p>Requires the Secretary to establish: (1) the Accelerated Approval Advisory Committee; (2) a new program to expand access to investigational treatments for individuals with serious or life threatening conditions and diseases; and (3) a demonstration project under the Medicare program to pay for drugs, biological, products, and devices approved under this Act.</p><p>Amends title XVIII (Medicare) of the Social Security Act to revise the definition of &quot;medically accepted indication&quot; to provide for coverage of a covered Part D drug based on the sponsor's or organization's determination that the drug is for a medically accepted indication.</p><p>Requires the Secretary to consider the clinical judgment and risks to the patient from the disease or condition in evaluating the safety and effectiveness of drugs, biological products, and devices that treat serious or life-threatening diseases or conditions, including the evaluation of nonstatistical information.</p><p>Requires any committee evaluating investigational drugs, devices, or biological product applications to have at least two patient representatives as voting members.</p>]]></text>
      </summary>
    </summaries>
    <title>Access, Compassion, Care, and Ethics for Seriously Ill Patients Act</title>
    <titles>
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        <titleType>Short Titles as Introduced</titleType>
        <title>Access, Compassion, Care, and Ethics for Seriously Ill Patients Act</title>
      </item>
      <item>
        <titleType>Short Titles as Introduced</titleType>
        <title>ACCESS Act</title>
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      <item>
        <titleType>Display Title</titleType>
        <title>Access, Compassion, Care, and Ethics for Seriously Ill Patients Act</title>
      </item>
      <item>
        <titleType>Official Title as Introduced</titleType>
        <title>To amend the Federal Food, Drug, and Cosmetic Act to create a new conditional approval system for drugs, biological products, and devices that is responsive to the needs of seriously ill patients, and for other purposes.</title>
      </item>
    </titles>
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        <type>Introduced in House</type>
        <date>2008-06-12T04:00:00Z</date>
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            <url>https://www.govinfo.gov/content/pkg/BILLS-110hr6270ih/xml/BILLS-110hr6270ih.xml</url>
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    <latestAction>
      <actionDate>2008-06-17</actionDate>
      <text>Referred to the Subcommittee on Health.</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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