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  <bill>
    <number>4790</number>
    <updateDate>2023-01-14T22:48:15Z</updateDate>
    <updateDateIncludingText>2023-01-14T22:48:15Z</updateDateIncludingText>
    <originChamber>House</originChamber>
    <originChamberCode>H</originChamberCode>
    <type>HR</type>
    <introducedDate>2004-07-09</introducedDate>
    <congress>108</congress>
    <committees>
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        <systemCode>hsif00</systemCode>
        <name>Energy and Commerce Committee</name>
        <chamber>House</chamber>
        <type>Standing</type>
        <subcommittees>
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            <systemCode>hsif14</systemCode>
            <name>Health Subcommittee</name>
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              <item>
                <name>Referred to</name>
                <date>2004-07-19T15:58:33Z</date>
              </item>
            </activities>
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            <name>Referred to</name>
            <date>2004-07-09T13:01:10Z</date>
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        <actionDate>2004-07-19</actionDate>
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            <name>Health Subcommittee</name>
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        <text>Referred to the Subcommittee on Health.</text>
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        <actionDate>2004-07-09</actionDate>
        <text>Referred to the House Committee on Energy and Commerce.</text>
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        <text>Introduced in House</text>
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        <actionDate>2004-07-09</actionDate>
        <text>Introduced in House</text>
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    <sponsors>
      <item>
        <bioguideId>J000110</bioguideId>
        <fullName>Rep. John, Christopher [D-LA-7]</fullName>
        <firstName>CHRISTOPHER</firstName>
        <lastName>JOHN</lastName>
        <party>D</party>
        <state>LA</state>
        <district>7</district>
        <isByRequest>N</isByRequest>
      </item>
    </sponsors>
    <policyArea>
      <name>Health</name>
    </policyArea>
    <subjects>
      <legislativeSubjects>
        <item>
          <name>Accreditation (Medical care)</name>
        </item>
        <item>
          <name>Administrative procedure</name>
        </item>
        <item>
          <name>Administrative remedies</name>
        </item>
        <item>
          <name>Advertising</name>
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        <item>
          <name>Australia</name>
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        <item>
          <name>Business records</name>
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        <item>
          <name>Canada</name>
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          <name>Charitable contributions</name>
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          <name>Civil Rights and Liberties, Minority Issues</name>
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          <name>Commerce</name>
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          <name>Communication in medicine</name>
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        <item>
          <name>Congress</name>
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        <item>
          <name>Congressional reporting requirements</name>
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        <item>
          <name>Consumer education</name>
        </item>
        <item>
          <name>Deceptive advertising</name>
        </item>
        <item>
          <name>Defective products</name>
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        <item>
          <name>Department of Health and Human Services</name>
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        <item>
          <name>Directories</name>
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        <item>
          <name>Drug abuse</name>
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        <item>
          <name>Drug industry</name>
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          <name>Drug interactions</name>
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        <item>
          <name>Drugs</name>
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        <item>
          <name>East Asia</name>
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          <name>Economics and Public Finance</name>
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        <item>
          <name>Electronic commerce</name>
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        <item>
          <name>Electronic data interchange</name>
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        <item>
          <name>Electronic government information</name>
        </item>
        <item>
          <name>Europe</name>
        </item>
        <item>
          <name>European Union</name>
        </item>
        <item>
          <name>Executive reorganization</name>
        </item>
        <item>
          <name>Food and Drug Administration (FDA)</name>
        </item>
        <item>
          <name>Foreign Trade and International Finance</name>
        </item>
        <item>
          <name>Government Operations and Politics</name>
        </item>
        <item>
          <name>Government contractors</name>
        </item>
        <item>
          <name>Government paperwork</name>
        </item>
        <item>
          <name>Government publicity</name>
        </item>
        <item>
          <name>Governmental investigations</name>
        </item>
        <item>
          <name>Grants-in-aid</name>
        </item>
        <item>
          <name>Health information systems</name>
        </item>
        <item>
          <name>Identification devices</name>
        </item>
        <item>
          <name>Import restrictions</name>
        </item>
        <item>
          <name>Imports</name>
        </item>
        <item>
          <name>Injunctions</name>
        </item>
        <item>
          <name>Intellectual property</name>
        </item>
        <item>
          <name>Interactive media</name>
        </item>
        <item>
          <name>Internet</name>
        </item>
        <item>
          <name>Japan</name>
        </item>
        <item>
          <name>Labeling</name>
        </item>
        <item>
          <name>Law</name>
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        <item>
          <name>Liability (Law)</name>
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        <item>
          <name>Licenses</name>
        </item>
        <item>
          <name>Medical records</name>
        </item>
        <item>
          <name>Medication abuse</name>
        </item>
        <item>
          <name>New Zealand</name>
        </item>
        <item>
          <name>Oceania</name>
        </item>
        <item>
          <name>Packaging</name>
        </item>
        <item>
          <name>Patients' rights</name>
        </item>
        <item>
          <name>Performance measurement</name>
        </item>
        <item>
          <name>Pharmacies</name>
        </item>
        <item>
          <name>Pharmacists</name>
        </item>
        <item>
          <name>Physicians</name>
        </item>
        <item>
          <name>Prescription pricing</name>
        </item>
        <item>
          <name>Product counterfeiting</name>
        </item>
        <item>
          <name>Product safety</name>
        </item>
        <item>
          <name>Right of privacy</name>
        </item>
        <item>
          <name>Science, Technology, Communications</name>
        </item>
        <item>
          <name>Switzerland</name>
        </item>
        <item>
          <name>Telephone</name>
        </item>
        <item>
          <name>Web sites</name>
        </item>
        <item>
          <name>Wholesale trade</name>
        </item>
      </legislativeSubjects>
      <policyArea>
        <name>Health</name>
      </policyArea>
    </subjects>
    <summaries>
      <summary>
        <versionCode>00</versionCode>
        <actionDate>2004-07-09</actionDate>
        <actionDesc>Introduced in House</actionDesc>
        <updateDate>2005-01-10T15:44:48Z</updateDate>
        <text><![CDATA[ <p>Drug Importation Promotion and Safety Act - Amends the Federal Food, Drug, and Cosmetic Act to establish the Office of Drug Importation Promotion and Safety.</p> <p>Allows a registered drug importation facility, pharmacy, Internet pharmacy, or wholesaler to import a Food and Drug Administration (FDA)-approved prescription drug from Canada or a permitted country.</p> <p>Prohibits the commingling of domestic and imported prescription drugs.</p> <p>Requires a pharmacy or Internet pharmacy that dispenses an imported prescription drug to label such drug accordingly.</p> <p>Allows individuals to import prescription drugs from: (1) a registered Internet pharmacy; or (2) licensed pharmacies for personal use.</p> <p>Allows the Secretary to suspend importation of a particular drug from a particular facility, pharmacy, wholesaler, or country.</p> <p>Allows licensed Internet pharmacies to dispense prescription drugs. Sets forth licensing requirements for Internet pharmacies.</p> <p>Makes interactive computer service providers and advertising service providers liable for violations under this Act if such a provider accepts advertising: (1) for a prescription drug from an unlicensed Internet pharmacy; or (2) stating that an individual does not need a prescription to obtain a prescription drug. </p> <p>Requires the Secretary to: (1) require the adoption and use of electronic track and trace technology to identify each sale, purchase, or trade of a prescription drug; and (2) establish a network to provide prompt notification of counterfeit drugs and to facilitate the identification and reporting of such drugs.</p> <p>Sets forth requirements for wholesalers, including requirements to identify the immediately previous distributor of record and all previous sales, purchases, or trades for imported prescription drugs.</p>]]></text>
      </summary>
    </summaries>
    <title>Drug Importation Promotion and Safety Act</title>
    <titles>
      <item>
        <titleType>Display Title</titleType>
        <title>Drug Importation Promotion and Safety Act</title>
      </item>
      <item>
        <titleType>Official Title as Introduced</titleType>
        <title>To amend the Federal Food, Drug, and Cosmetic Act to authorize the importation of prescription drugs from Canada and certain other countries, and for other purposes.</title>
        <billTextVersionName>Introduced in House</billTextVersionName>
        <billTextVersionCode>IH</billTextVersionCode>
      </item>
      <item>
        <titleType>Short Titles as Introduced</titleType>
        <title>Drug Importation Promotion and Safety Act</title>
      </item>
    </titles>
    <textVersions>
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        <type>Introduced in House</type>
        <date>2004-07-09T04:00:00Z</date>
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          <item>
            <url>https://www.govinfo.gov/content/pkg/BILLS-108hr4790ih/xml/BILLS-108hr4790ih.xml</url>
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    <latestAction>
      <actionDate>2004-07-19</actionDate>
      <text>Referred to the Subcommittee on Health.</text>
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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>
    <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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