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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">clinvest</journal-id><journal-title-group><journal-title xml:lang="ru">Качественная клиническая практика</journal-title><trans-title-group xml:lang="en"><trans-title>Kachestvennaya Klinicheskaya Praktika = Good Clinical Practice</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2588-0519</issn><issn pub-type="epub">2618-8473</issn><publisher><publisher-name>ООО «Издательство ОКИ</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">clinvest-137</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>НЕИНТЕРВЕНЦИОННЫЕ ИССЛЕДОВАНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>NON-INTERVENTIONAL STUDY</subject></subj-group></article-categories><title-group><article-title>Основы надлежащей практики неинтервенционных исследований лекарственных препаратов</article-title><trans-title-group xml:lang="en"><trans-title></trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Вольская</surname><given-names>Е. А.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кафедра управления здравоохранением и лекарственного менеджмента</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff xml:lang="ru" id="aff-1"><institution>Первого МГМУ им. И.М. Сеченова, г. Москва</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2011</year></pub-date><pub-date pub-type="epub"><day>05</day><month>06</month><year>2018</year></pub-date><volume>0</volume><issue>1</issue><fpage>19</fpage><lpage>24</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Вольская Е.А., 2018</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="ru">Вольская Е.А.</copyright-holder><copyright-holder xml:lang="en">Вольская Е.А.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.clinvest.ru/jour/article/view/137">https://www.clinvest.ru/jour/article/view/137</self-uri><abstract/><kwd-group xml:lang="ru"><kwd>неинтервенционные исследования</kwd><kwd>регулирование</kwd><kwd>этическая экспертиза</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Федеральный закон от 12.04.2010 г. № 61-ФЗ «Об обращении лекарственных средств».</mixed-citation><mixed-citation xml:lang="en">Федеральный закон от 12.04.2010 г. № 61-ФЗ «Об обращении лекарственных средств».</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Национальный стандарт РФ ГОСТ-Р 52379—2005 «Надлежащая клиническая практика» (ICH E6 GCP), утвержденный приказом Федерального агентства по техническому регулированию и метрологии от 27.09.2005 № 232-ст.</mixed-citation><mixed-citation xml:lang="en">Национальный стандарт РФ ГОСТ-Р 52379—2005 «Надлежащая клиническая практика» (ICH E6 GCP), утвержденный приказом Федерального агентства по техническому регулированию и метрологии от 27.09.2005 № 232-ст.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Guideline for Good Clinical Practice E6 (R1).</mixed-citation><mixed-citation xml:lang="en">Guideline for Good Clinical Practice E6 (R1).</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use.</mixed-citation><mixed-citation xml:lang="en">Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">EFPIA Code on the Promotion of prescription-only Medicines to, and Interactions with healthcare Professionals.//http://www.efpia. org/Content/Default.asp?PageID=366</mixed-citation><mixed-citation xml:lang="en">EFPIA Code on the Promotion of prescription-only Medicines to, and Interactions with healthcare Professionals.//http://www.efpia. org/Content/Default.asp?PageID=366</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Empfehlungen des Bundesinstituts für Arzneimittel und Medizinprodukte und des Paul-Ehrlich-Instituts zur Planung, Durchführung und Auswertung von Anwendungsbeobachtungen.7. 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