{"id":290,"date":"2021-06-15T11:08:48","date_gmt":"2021-06-15T11:08:48","guid":{"rendered":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?post_type=event&p=290"},"modified":"2021-06-15T11:23:34","modified_gmt":"2021-06-15T11:23:34","slug":"usfda-iacra-webinar-series-on-medical-device-iso-13485-and-mdsap","status":"publish","type":"event","link":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/coalition-action\/events\/usfda-iacra-webinar-series-on-medical-device-iso-13485-and-mdsap\/","title":{"rendered":"USFDA – IACRA Webinar Series on Medical Device: ISO 13485 and MDSAP"},"content":{"rendered":"\n

The United States Food and Drug Administration (FDA) with the support of the Medical Device Regulatory Convergence Project<\/a> co-lead by USAID, ANSI, and AdvaMed through the Inter-American Coalition for Regulatory Convergence in the Medical Technology Sector<\/a>, organized a series of webinar sessions on ISO 13485 and Medical Device Single Audit Program (MDSAP) outcomes utilization for regulatory purposes, where ANVISA and ANMAT, besides the USFDA share their experiences.<\/p>\n","protected":false},"featured_media":0,"parent":0,"template":"","event_category":[10],"class_list":["post-290","event","type-event","status-publish","hentry","event_category-public","event_category-10","description-off"],"acf":[],"yoast_head":"\nUSFDA - IACRA Webinar Series on Medical Device: ISO 13485 and MDSAP - 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\/coalition-action\/events\/usfda-iacra-webinar-series-on-medical-device-iso-13485-and-mdsap\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"USFDA - IACRA Webinar Series on Medical Device: ISO 13485 and MDSAP - Regulatory Convergence\" \/>\n<meta property=\"og:description\" content=\"The United States Food and Drug Administration (FDA) with the support of the Medical Device Regulatory Convergence Project co-lead by USAID, ANSI, and AdvaMed through the Inter-American Coalition for Regulatory Convergence in the Medical Technology Sector, organized a series of webinar sessions on ISO 13485 and Medical Device Single Audit Program (MDSAP) outcomes utilization for…\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/coalition-action\/events\/usfda-iacra-webinar-series-on-medical-device-iso-13485-and-mdsap\/\" \/>\n<meta property=\"og:site_name\" content=\"Regulatory Convergence\" \/>\n<meta property=\"article:modified_time\" content=\"2021-06-15T11:23:34+00:00\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/coalition-action\\\/events\\\/usfda-iacra-webinar-series-on-medical-device-iso-13485-and-mdsap\\\/\",\"url\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/coalition-action\\\/events\\\/usfda-iacra-webinar-series-on-medical-device-iso-13485-and-mdsap\\\/\",\"name\":\"USFDA - IACRA Webinar Series on Medical Device: ISO 13485 and MDSAP - Regulatory Convergence\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/?lang=es\\\/#website\"},\"datePublished\":\"2021-06-15T11:08:48+00:00\",\"dateModified\":\"2021-06-15T11:23:34+00:00\",\"breadcrumb\":{\"@id\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/coalition-action\\\/events\\\/usfda-iacra-webinar-series-on-medical-device-iso-13485-and-mdsap\\\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/coalition-action\\\/events\\\/usfda-iacra-webinar-series-on-medical-device-iso-13485-and-mdsap\\\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/coalition-action\\\/events\\\/usfda-iacra-webinar-series-on-medical-device-iso-13485-and-mdsap\\\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Events\",\"item\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/coalition-action\\\/events\\\/\"},{\"@type\":\"ListItem\",\"position\":3,\"name\":\"USFDA – IACRA Webinar Series on Medical Device: ISO 13485 and MDSAP\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/?lang=es\\\/#website\",\"url\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/?lang=es\\\/\",\"name\":\"Regulatory Convergence\",\"description\":\"Inter-American Coalition\",\"publisher\":{\"@id\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/?lang=es\\\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/?lang=es\\\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"},{\"@type\":\"Organization\",\"@id\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/?lang=es\\\/#organization\",\"name\":\"Inter-American Coalition - Regulatory Convergence\",\"url\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/?lang=es\\\/\",\"logo\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/?lang=es\\\/#\\\/schema\\\/logo\\\/image\\\/\",\"url\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/wp-content\\\/uploads\\\/sites\\\/4\\\/2021\\\/07\\\/logo_regulatory_retina_en.png\",\"contentUrl\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/wp-content\\\/uploads\\\/sites\\\/4\\\/2021\\\/07\\\/logo_regulatory_retina_en.png\",\"width\":559,\"height\":280,\"caption\":\"Inter-American Coalition - Regulatory Convergence\"},\"image\":{\"@id\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/?lang=es\\\/#\\\/schema\\\/logo\\\/image\\\/\"}}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"USFDA - IACRA Webinar Series on Medical Device: ISO 13485 and MDSAP - Regulatory Convergence","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/coalition-action\/events\/usfda-iacra-webinar-series-on-medical-device-iso-13485-and-mdsap\/","og_locale":"en_US","og_type":"article","og_title":"USFDA - IACRA Webinar Series on Medical Device: ISO 13485 and MDSAP - Regulatory Convergence","og_description":"The United States Food and Drug Administration (FDA) with the support of the Medical Device Regulatory Convergence Project co-lead by USAID, ANSI, and AdvaMed through the Inter-American Coalition for Regulatory Convergence in the Medical Technology Sector, organized a series of webinar sessions on ISO 13485 and Medical Device Single Audit Program (MDSAP) outcomes utilization for…","og_url":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/coalition-action\/events\/usfda-iacra-webinar-series-on-medical-device-iso-13485-and-mdsap\/","og_site_name":"Regulatory Convergence","article_modified_time":"2021-06-15T11:23:34+00:00","twitter_card":"summary_large_image","twitter_misc":{"Est. reading time":"1 minute"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/coalition-action\/events\/usfda-iacra-webinar-series-on-medical-device-iso-13485-and-mdsap\/","url":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/coalition-action\/events\/usfda-iacra-webinar-series-on-medical-device-iso-13485-and-mdsap\/","name":"USFDA - IACRA Webinar Series on Medical Device: ISO 13485 and MDSAP - Regulatory Convergence","isPartOf":{"@id":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/#website"},"datePublished":"2021-06-15T11:08:48+00:00","dateModified":"2021-06-15T11:23:34+00:00","breadcrumb":{"@id":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/coalition-action\/events\/usfda-iacra-webinar-series-on-medical-device-iso-13485-and-mdsap\/#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/coalition-action\/events\/usfda-iacra-webinar-series-on-medical-device-iso-13485-and-mdsap\/"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/coalition-action\/events\/usfda-iacra-webinar-series-on-medical-device-iso-13485-and-mdsap\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/"},{"@type":"ListItem","position":2,"name":"Events","item":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/coalition-action\/events\/"},{"@type":"ListItem","position":3,"name":"USFDA – IACRA Webinar Series on Medical Device: ISO 13485 and MDSAP"}]},{"@type":"WebSite","@id":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/#website","url":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/","name":"Regulatory Convergence","description":"Inter-American Coalition","publisher":{"@id":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/#organization"},"potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"en-US"},{"@type":"Organization","@id":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/#organization","name":"Inter-American Coalition - Regulatory Convergence","url":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/","logo":{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/#\/schema\/logo\/image\/","url":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2021\/07\/logo_regulatory_retina_en.png","contentUrl":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2021\/07\/logo_regulatory_retina_en.png","width":559,"height":280,"caption":"Inter-American Coalition - Regulatory Convergence"},"image":{"@id":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/#\/schema\/logo\/image\/"}}]}},"uagb_featured_image_src":{"full":false,"thumbnail":false,"medium":false,"medium_large":false,"large":false,"1536x1536":false,"2048x2048":false},"uagb_author_info":{"display_name":"Guilherme Guain","author_link":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/author\/"},"uagb_comment_info":0,"uagb_excerpt":"The United States Food and Drug Administration (FDA) with the support of the Medical Device Regulatory Convergence Project co-lead by USAID, ANSI, and AdvaMed through the Inter-American Coalition for Regulatory Convergence in the Medical Technology Sector, organized a series of webinar sessions on ISO 13485 and Medical Device Single Audit Program (MDSAP) outcomes utilization for…","_links":{"self":[{"href":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-json\/wp\/v2\/event\/290","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-json\/wp\/v2\/event"}],"about":[{"href":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-json\/wp\/v2\/types\/event"}],"wp:attachment":[{"href":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-json\/wp\/v2\/media?parent=290"}],"wp:term":[{"taxonomy":"event_category","embeddable":true,"href":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-json\/wp\/v2\/event_category?post=290"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}