{"id":2562,"date":"2021-08-11T19:07:18","date_gmt":"2021-08-11T19:07:18","guid":{"rendered":"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/?post_type=regulator-sessions&#038;p=2562"},"modified":"2024-01-18T12:15:36","modified_gmt":"2024-01-18T12:15:36","slug":"u-s-food-and-drug-administration-latam-office","status":"publish","type":"policy-training","link":"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/policy-training\/u-s-food-and-drug-administration-latam-office\/","title":{"rendered":"U.S. Food and Drug Administration \u2013 LatAm Office"},"content":{"rendered":"\n<p>U.S. FDA Latin America Office, IMDRF: WGs and Priorities, MD Division (CDRH) &amp; LatAm Activities, FDA Standards &amp; Conformity Program\/Policy and MDSAP &amp; ISO13485.<\/p>\n\n\n\n<p class=\"mb-3\"><a href=\"http:\/\/staging.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>,&nbsp;<a href=\"http:\/\/staging.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>,&nbsp;<a href=\"http:\/\/staging.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>,&nbsp;<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>The Center for Devices and Radiological Health (CDRH) \u2013 FDA provides a web page for multimedia industry education. The modules&nbsp; available describe many aspects of medical device regulations covering both premarket and postmarket topics.<\/p>\n\n\n\n<p>To know more about CDHR Learn,&nbsp;<a href=\"https:\/\/www.fda.gov\/training-and-continuing-education\/cdrh-learn\" target=\"_blank\" rel=\"noreferrer noopener\">click here<\/a>.<\/p>\n\n\n\n<p>You may find CDHR Learn resources in Spanish&nbsp;<a href=\"https:\/\/www.fda.gov\/training-and-continuing-education\/cdrh-learn\/cdrh-learn-course-list-spanish\" target=\"_blank\" rel=\"noreferrer noopener\">here<\/a>.<\/p>\n","protected":false},"parent":0,"menu_order":0,"template":"","event_category":[],"class_list":["post-2562","policy-training","type-policy-training","status-publish","hentry","description-off"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.4 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>U.S. Food and Drug Administration \u2013 LatAm Office - 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:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/policy-training\/u-s-food-and-drug-administration-latam-office\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"U.S. Food and Drug Administration \u2013 LatAm Office - Regulatory Convergence\" \/>\n<meta property=\"og:description\" content=\"U.S. FDA Latin America Office, IMDRF: WGs and Priorities, MD Division (CDRH) &amp; LatAm Activities, FDA Standards &amp; Conformity Program\/Policy and MDSAP &amp; ISO13485. Agenda,&nbsp;Slides Deck,&nbsp;FDA Presentation \u2013 Talking Points,&nbsp;Webinar Recording U.S. Food and Drug Administration The Center for Devices and Radiological Health (CDRH) \u2013 FDA provides a web page for multimedia industry education. 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Agenda,&nbsp;Slides Deck,&nbsp;FDA Presentation \u2013 Talking Points,&nbsp;Webinar Recording U.S. Food and Drug Administration The Center for Devices and Radiological Health (CDRH) \u2013 FDA provides a web page for multimedia industry education. The&hellip;","og_url":"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/policy-training\/u-s-food-and-drug-administration-latam-office\/","og_site_name":"Regulatory Convergence","article_modified_time":"2024-01-18T12:15:36+00:00","twitter_card":"summary_large_image","twitter_misc":{"Est. reading time":"1 minute"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/policy-training\/u-s-food-and-drug-administration-latam-office\/","url":"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/policy-training\/u-s-food-and-drug-administration-latam-office\/","name":"U.S. Food and Drug Administration \u2013 LatAm Office - Regulatory Convergence","isPartOf":{"@id":"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/#website"},"datePublished":"2021-08-11T19:07:18+00:00","dateModified":"2024-01-18T12:15:36+00:00","breadcrumb":{"@id":"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/policy-training\/u-s-food-and-drug-administration-latam-office\/#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/policy-training\/u-s-food-and-drug-administration-latam-office\/"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/policy-training\/u-s-food-and-drug-administration-latam-office\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/"},{"@type":"ListItem","position":2,"name":"Policy Training","item":"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/policy-training\/"},{"@type":"ListItem","position":3,"name":"U.S. Food and Drug Administration \u2013 LatAm Office"}]},{"@type":"WebSite","@id":"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/#website","url":"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/","name":"Regulatory Convergence","description":"Inter-American Coalition","potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"en-US"}]}},"uagb_featured_image_src":[],"uagb_author_info":{"display_name":"Guilherme Guain","author_link":"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/author\/"},"uagb_comment_info":0,"uagb_excerpt":"U.S. FDA Latin America Office, IMDRF: WGs and Priorities, MD Division (CDRH) &amp; LatAm Activities, FDA Standards &amp; Conformity Program\/Policy and MDSAP &amp; ISO13485. Agenda,&nbsp;Slides Deck,&nbsp;FDA Presentation \u2013 Talking Points,&nbsp;Webinar Recording U.S. Food and Drug Administration The Center for Devices and Radiological Health (CDRH) \u2013 FDA provides a web page for multimedia industry education. 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