<section xmlns="http://xml.house.gov/schemas/uslm/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" style="-uslm-lc:I80" id="id29310d9a-09a0-11eb-a78d-da6bfa680960" identifier="/us/usc/t21/s383"><num value="383">§ 383.</num><heading> Office of International Relations</heading><subsection style="-uslm-lc:I19" class="indent2 firstIndent-2" id="id29310d9b-09a0-11eb-a78d-da6bfa680960" identifier="/us/usc/t21/s383/a"><num value="a" class="bold">(a)</num><heading class="bold"> Establishment</heading><content><p style="-uslm-lc:I11" class="indent0">There is established in the Department of Health and Human Services an Office of International Relations.</p>
</content>
</subsection>
<subsection style="-uslm-lc:I19" class="indent2 firstIndent-2" id="id29310d9c-09a0-11eb-a78d-da6bfa680960" identifier="/us/usc/t21/s383/b"><num value="b" class="bold">(b)</num><heading class="bold"> Agreements with foreign countries</heading><chapeau style="-uslm-lc:I11" class="indent0">In carrying out the functions of the office under subsection (a), the Secretary may enter into agreements with foreign countries to facilitate commerce in devices between the United States and such countries consistent with the requirements of this chapter. In such agreements, the Secretary shall encourage the mutual recognition of—</chapeau><paragraph style="-uslm-lc:I12" class="indent1" id="id29310d9d-09a0-11eb-a78d-da6bfa680960" identifier="/us/usc/t21/s383/b/1"><num value="1">(1)</num><content> good manufacturing practice regulations promulgated under <ref href="/us/usc/t21/s360j/f">section 360j(f) of this title</ref>, and</content>
</paragraph>
<paragraph style="-uslm-lc:I12" class="indent1" id="id29310d9e-09a0-11eb-a78d-da6bfa680960" identifier="/us/usc/t21/s383/b/2"><num value="2">(2)</num><content> other regulations and testing protocols as the Secretary determines to be appropriate.</content>
</paragraph>
</subsection>
<subsection style="-uslm-lc:I19" class="indent2 firstIndent-2" id="id29310d9f-09a0-11eb-a78d-da6bfa680960" identifier="/us/usc/t21/s383/c"><num value="c" class="bold">(c)</num><heading class="bold"> Harmonizing regulatory requirements</heading><paragraph style="-uslm-lc:I11" class="indent0" id="id29310da0-09a0-11eb-a78d-da6bfa680960" identifier="/us/usc/t21/s383/c/1"><num value="1">(1)</num><content> The Secretary shall support the Office of the United States Trade Representative, in consultation with the Secretary of Commerce, in meetings with representatives of other countries to discuss methods and approaches to reduce the burden of regulation and harmonize regulatory requirements if the Secretary determines that such harmonization continues consumer protections consistent with the purposes of this chapter.</content>
</paragraph>
<paragraph style="-uslm-lc:I11" class="indent0" id="id29310da1-09a0-11eb-a78d-da6bfa680960" identifier="/us/usc/t21/s383/c/2"><num value="2">(2)</num><content> The Secretary shall support the Office of the United States Trade Representative, in consultation with the Secretary of Commerce, in efforts to move toward the acceptance of mutual recognition agreements relating to the regulation of drugs, biological products, devices, foods, food additives, and color additives, and the regulation of good manufacturing practices, between the European Union and the United States.</content>
</paragraph>
<paragraph style="-uslm-lc:I11" class="indent0" id="id29310da2-09a0-11eb-a78d-da6bfa680960" identifier="/us/usc/t21/s383/c/3"><num value="3">(3)</num><subparagraph style="-uslm-lc:I11" class="indent0" id="id29310da3-09a0-11eb-a78d-da6bfa680960" identifier="/us/usc/t21/s383/c/3/A"><num value="A">(A)</num><content> The Secretary shall regularly participate in meetings with representatives of other foreign governments to discuss and reach agreement on methods and approaches to harmonize regulatory requirements.</content>
</subparagraph>
<subparagraph style="-uslm-lc:I11" class="indent0" id="id29310da4-09a0-11eb-a78d-da6bfa680960" identifier="/us/usc/t21/s383/c/3/B"><num value="B">(B)</num><chapeau> In carrying out subparagraph (A), the Secretary may participate in appropriate fora, including the International Medical Device Regulators Forum, and may—</chapeau><clause style="-uslm-lc:I12" class="indent1" id="id29310da5-09a0-11eb-a78d-da6bfa680960" identifier="/us/usc/t21/s383/c/3/B/i"><num value="i">(i)</num><content> provide guidance to such fora on strategies, policies, directions, membership, and other activities of a forum as appropriate;</content>
</clause>
<clause style="-uslm-lc:I12" class="indent1" id="id29310da6-09a0-11eb-a78d-da6bfa680960" identifier="/us/usc/t21/s383/c/3/B/ii"><num value="ii">(ii)</num><content> to the extent appropriate, solicit, review, and consider comments from industry, academia, health care professionals, and patient groups regarding the activities of such fora; and</content>
</clause>
<clause style="-uslm-lc:I12" class="indent1" id="id293134b7-09a0-11eb-a78d-da6bfa680960" identifier="/us/usc/t21/s383/c/3/B/iii"><num value="iii">(iii)</num><content> to the extent appropriate, inform the public of the Secretary’s activities within such fora, and share with the public any documentation relating to a forum’s strategies, policies, and other activities of such fora.</content>
</clause>
</subparagraph>
</paragraph>
<paragraph style="-uslm-lc:I11" class="indent0" id="id293134b8-09a0-11eb-a78d-da6bfa680960" identifier="/us/usc/t21/s383/c/4"><num value="4">(4)</num><content> With respect to devices, the Secretary may, when appropriate, enter into arrangements with nations regarding methods and approaches to harmonizing regulatory requirements for activities, including inspections and common international labeling symbols.</content>
</paragraph>
<paragraph style="-uslm-lc:I11" class="indent0" id="id293134b9-09a0-11eb-a78d-da6bfa680960" identifier="/us/usc/t21/s383/c/5"><num value="5">(5)</num><content> Paragraphs (1) through (4) shall not apply with respect to products defined in <ref href="/us/usc/t21/s321/ff">section 321(ff) of this title</ref>.</content>
</paragraph>
</subsection>
<sourceCredit id="id293134ba-09a0-11eb-a78d-da6bfa680960">(<ref href="/us/act/1938-06-25/ch675/s803">June 25, 1938, ch. 675, § 803</ref>, as added <ref href="/us/pl/101/629/s15/a">Pub. L. 101–629, § 15(a)</ref>, <date date="1990-11-28">Nov. 28, 1990</date>, <ref href="/us/stat/104/4525">104 Stat. 4525</ref>; amended <ref href="/us/pl/105/115/tIV/s410/b">Pub. L. 105–115, title IV, § 410(b)</ref>, <date date="1997-11-21">Nov. 21, 1997</date>, <ref href="/us/stat/111/2373">111 Stat. 2373</ref>; <ref href="/us/pl/112/144/tVI">Pub. L. 112–144, title VI</ref>, §§ 609, 610, <date date="2012-07-09">July 9, 2012</date>, <ref href="/us/stat/126/1059">126 Stat. 1059</ref>.)</sourceCredit>
<notes type="uscNote" id="id293134bb-09a0-11eb-a78d-da6bfa680960">
<note style="-uslm-lc:I74" topic="amendments" id="id293134bc-09a0-11eb-a78d-da6bfa680960"><heading class="centered smallCaps">Amendments</heading><p style="-uslm-lc:I21" class="indent0">2012—Subsec. (c)(3). <ref href="/us/pl/112/144/s610">Pub. L. 112–144, § 610</ref>, designated existing provisions as subpar. (A) and added subpar. (B).</p>
<p style="-uslm-lc:I21" class="indent0">Subsec. (c)(4). <ref href="/us/pl/112/144/s609">Pub. L. 112–144, § 609</ref>, amended par. (4) generally. Prior to amendment, par. (4) read as follows: “The Secretary shall, not later than 180 days after <date date="1997-11-21">November 21, 1997</date>, make public a plan that establishes a framework for achieving mutual recognition of good manufacturing practices inspections.”</p>
<p style="-uslm-lc:I21" class="indent0">1997—Subsec. (c). <ref href="/us/pl/105/115">Pub. L. 105–115</ref> added subsec. (c).</p>
</note>
<note style="-uslm-lc:I74" topic="effectiveDateOfAmendment" id="id293134bd-09a0-11eb-a78d-da6bfa680960"><heading class="centered smallCaps">Effective Date of 1997 Amendment</heading><p style="-uslm-lc:I21" class="indent0">Amendment by <ref href="/us/pl/105/115">Pub. L. 105–115</ref> effective 90 days after <date date="1997-11-21">Nov. 21, 1997</date>, except as otherwise provided, see <ref href="/us/pl/105/115/s501">section 501 of Pub. L. 105–115</ref>, set out as a note under <ref href="/us/usc/t21/s321">section 321 of this title</ref>.</p>
</note>
<note style="-uslm-lc:I74" topic="miscellaneous" id="id293134be-09a0-11eb-a78d-da6bfa680960"><heading class="centered smallCaps">Report on Activities of Office of International Relations</heading><p style="-uslm-lc:I21" class="indent0"><ref href="/us/pl/101/629/s15/b">Pub. L. 101–629, § 15(b)</ref>, <date date="1990-11-28">Nov. 28, 1990</date>, <ref href="/us/stat/104/4525">104 Stat. 4525</ref>, directed Secretary of Health and Human Services, not later than 2 years after <date date="1990-11-28">Nov. 28, 1990</date>, to prepare and submit to the appropriate committees of Congress a report on the activities of the Office of International Relations under <ref href="/us/usc/t21/s383">21 U.S.C. 383</ref>.</p>
</note>
</notes>
</section>