{"id":2596,"date":"2021-08-13T13:31:16","date_gmt":"2021-08-13T13:31:16","guid":{"rendered":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/regulator-sessions\/administracion-de-alimentos-y-farmacos-de-los-ee-uu-oficina-de-america-latina\/"},"modified":"2021-08-13T13:35:14","modified_gmt":"2021-08-13T13:35:14","slug":"administracion-de-alimentos-y-farmacos-de-los-ee-uu-oficina-de-america-latina","status":"publish","type":"regulator-sessions","link":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/regulator-sessions\/administracion-de-alimentos-y-farmacos-de-los-ee-uu-oficina-de-america-latina\/?lang=es","title":{"rendered":"Administraci\u00f3n de Alimentos y F\u00e1rmacos de los EE. UU. \u2013 Oficina de Am\u00e9rica Latina"},"content":{"rendered":"\n<p>Oficina de Am\u00e9rica Latina de la FDA de los EE. UU., IMDRF: WGs y prioridades, Divisi\u00f3n MD (CDRH) y actividades en Am\u00e9rica Latina, Programa \/ Pol\u00edtica de normas y conformidad de la FDA y MDSAP e ISO13485.<\/p>\n\n\n\n<p class=\"mb-3\"><a href=\"http:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2021\/06\/Agenda-Policy-Session-with-Regulators-FDA-IACRCMTS-Fina-21May20.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">Agenda<\/a>, <a href=\"http:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2021\/06\/Slides-Deck-Webinar-4-Policy-USFDA.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">Slides Deck<\/a>, <a href=\"http:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2021\/06\/Medical-Devices-Regulatory-Convergence-eng-tp.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">FDA Presentation \u2013 Talking Points<\/a>, <a href=\"https:\/\/www.youtube.com\/watch?v=eYIO1gndvj4\" target=\"_blank\" rel=\"noreferrer noopener\">Webinar Recording<\/a><\/p>\n\n\n\n<p><strong>U.S. Food and Drug Administration<\/strong><\/p>\n\n\n\n<p>El Centro de Dispositivos y Salud Radiol\u00f3gica (CDRH) \u2013 FDA proporciona un sitio de internet para la educaci\u00f3n de la industria multimedia. Los m\u00f3dulos disponibles describen muchos aspectos de las regulaciones de dispositivos m\u00e9dicos que cubren temas tanto previos como posteriores a la comercializaci\u00f3n.<\/p>\n\n\n\n<p>Para conocer m\u00e1s de CDRH Learn, haz <a href=\"https:\/\/www.fda.gov\/training-and-continuing-education\/cdrh-learn\" target=\"_blank\" rel=\"noreferrer noopener\">click aqu\u00ed<\/a>.<\/p>\n\n\n\n<p>Puedes encontrar recursos en espa\u00f1ol de CDHR Learn haciendo <a href=\"https:\/\/www.fda.gov\/training-and-continuing-education\/cdrh-learn\/cdrh-learn-course-list-spanish\" target=\"_blank\" rel=\"noreferrer noopener\">click aqu\u00ed<\/a>.<\/p>\n","protected":false},"parent":0,"template":"","event_category":[],"class_list":["post-2596","regulator-sessions","type-regulator-sessions","status-publish","hentry","description-off"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Administraci\u00f3n de Alimentos y F\u00e1rmacos de los EE. UU. \u2013 Oficina de Am\u00e9rica Latina - Regulatory Convergence<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/regulator-sessions\/administracion-de-alimentos-y-farmacos-de-los-ee-uu-oficina-de-america-latina\/?lang=es\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Administraci\u00f3n de Alimentos y F\u00e1rmacos de los EE. UU. \u2013 Oficina de Am\u00e9rica Latina - Regulatory Convergence\" \/>\n<meta property=\"og:description\" content=\"Oficina de Am\u00e9rica Latina de la FDA de los EE. UU., IMDRF: WGs y prioridades, Divisi\u00f3n MD (CDRH) y actividades en Am\u00e9rica Latina, Programa \/ Pol\u00edtica de normas y conformidad de la FDA y MDSAP e ISO13485. 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Agenda, Slides Deck, FDA Presentation \u2013 Talking Points, Webinar Recording U.S. Food and Drug Administration El Centro de&hellip;","_links":{"self":[{"href":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-json\/wp\/v2\/regulator-sessions\/2596","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-json\/wp\/v2\/regulator-sessions"}],"about":[{"href":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-json\/wp\/v2\/types\/regulator-sessions"}],"wp:attachment":[{"href":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-json\/wp\/v2\/media?parent=2596"}],"wp:term":[{"taxonomy":"event_category","embeddable":true,"href":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-json\/wp\/v2\/event_category?post=2596"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}