{"id":3491,"date":"2022-01-26T12:03:26","date_gmt":"2022-01-26T12:03:26","guid":{"rendered":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?post_type=regulator-sessions&p=3491"},"modified":"2022-02-21T12:51:58","modified_gmt":"2022-02-21T12:51:58","slug":"webinar-series-on-unique-device-identification","status":"publish","type":"regulator-sessions","link":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/regulator-sessions\/webinar-series-on-unique-device-identification\/","title":{"rendered":"Webinar Series on Unique Device Identification"},"content":{"rendered":"\n

The Medical Device Regulatory Convergence Project<\/a> co-lead by USAID, ANSI, and AdvaMed through the Inter-American Coalition for Regulatory Convergence<\/a> in the Medical Technology Sector collaborated with the United States Food and Drug Administration (FDA) to organize a webinar series on Unique Device Identification.<\/p>\n\n\n\n

Objective<\/strong>: Provide an overview of the requirements related to Unique Device Identification (UDI) and FDA\u2019s perspective and experience implementing these requirements<\/p>\n\n\n\n

Session I – 20 January 2022<\/strong><\/h2>\n\n\n\n

Agenda<\/h2>\n\n\n\n
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English<\/a><\/div>\n\n\n\n
Spanish<\/a><\/div>\n<\/div>\n\n\n\n

Recording<\/h2>\n\n\n\n
\n
English<\/a><\/div>\n\n\n\n
Spanish<\/a><\/div>\n\n\n\n
Portuguese<\/a><\/div>\n<\/div>\n\n\n\n

Presentations<\/h2>\n\n\n\n

Vision for Global UDI System:<\/strong><\/h3>\n\n\n\n

Indira Konduri, FDA<\/h3>\n\n\n\n
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English<\/a><\/div>\n\n\n\n
Spanish<\/a><\/div>\n\n\n\n
Portuguese<\/a><\/div>\n<\/div>\n\n\n\n

Helio Filho, ANVISA<\/h3>\n\n\n\n
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English<\/a><\/div>\n\n\n\n
Spanish<\/a><\/div>\n\n\n\n
Portuguese<\/a><\/div>\n<\/div>\n\n\n\n

Overview of UDI and IMDRF documents<\/strong><\/h3>\n\n\n\n
\n
English<\/a><\/div>\n\n\n\n
Spanish<\/a><\/div>\n\n\n\n
Portuguese<\/a><\/div>\n<\/div>\n\n\n\n

Session II – 27 January 2022<\/strong><\/h2>\n\n\n\n

Agenda<\/h2>\n\n\n\n
\n
English<\/a><\/div>\n\n\n\n
Spanish<\/a><\/div>\n<\/div>\n\n\n\n

Recording<\/h2>\n\n\n\n
\n
English<\/a><\/div>\n\n\n\n
Spanish<\/a><\/div>\n\n\n\n
Portuguese<\/a><\/div>\n<\/div>\n\n\n\n

Presentations<\/h2>\n\n\n\n

Industry Experience implementing UDIs: John Terwilliger, Abbott<\/h3>\n\n\n\n
\n
English<\/a><\/div>\n\n\n\n
Spanish<\/a><\/div>\n\n\n\n
Portuguese<\/a><\/div>\n<\/div>\n\n\n\n

Healthcare provider experience implementing UDIs: Cynthia Shumway \u2013 Intermountain Healthcare<\/h3>\n\n\n\n
\n
English<\/a><\/div>\n\n\n\n
Spanish<\/a><\/div>\n\n\n\n
Portuguese<\/a><\/div>\n<\/div>\n\n\n\n

Regulators Experiences:<\/strong><\/h3>\n\n\n\n

ANVISA \u2013 H\u00e9lio Filho<\/h3>\n\n\n\n
\n
English<\/a><\/div>\n\n\n\n
Spanish<\/a><\/div>\n\n\n\n
Portuguese<\/a><\/div>\n<\/div>\n\n\n\n

ARCSA \u2013 Xavier Quintero<\/h3>\n\n\n\n
\n
English<\/a><\/div>\n\n\n\n
Spanish<\/a><\/div>\n\n\n\n
Portuguese<\/a><\/div>\n<\/div>\n\n\n\n

FDA – Indira Konduri<\/h3>\n\n\n\n
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English<\/a><\/div>\n\n\n\n
Spanish<\/a><\/div>\n\n\n\n
Portuguese<\/a><\/div>\n<\/div>\n\n\n\n

Minsal \u2013 \u00d3scar Mar\u00edn<\/h3>\n\n\n\n
\n
English<\/a><\/div>\n\n\n\n
Spanish<\/a><\/div>\n\n\n\n
Portuguese<\/a><\/div>\n<\/div>\n","protected":false},"parent":0,"template":"","event_category":[],"class_list":["post-3491","regulator-sessions","type-regulator-sessions","status-publish","hentry","description-off"],"acf":[],"yoast_head":"\nWebinar Series on Unique Device Identification - 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\/webinar-series-on-unique-device-identification\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Webinar Series on Unique Device Identification - Regulatory Convergence\" \/>\n<meta property=\"og:description\" content=\"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 collaborated with the United States Food and Drug Administration (FDA) to organize a webinar series on Unique Device Identification. 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