{"id":11416,"date":"2023-03-20T17:10:48","date_gmt":"2023-03-20T16:10:48","guid":{"rendered":"https:\/\/biopmed.eu\/evento\/post-marketing-surveillance\/"},"modified":"2023-03-20T17:10:48","modified_gmt":"2023-03-20T16:10:48","slug":"post-marketing-surveillance","status":"publish","type":"tribe_events","link":"https:\/\/biopmed.eu\/en\/evento-en\/post-marketing-surveillance\/","title":{"rendered":"Post-marketing surveillance"},"content":{"rendered":"<h6><em>A webinar that offers an overview of post-market surveillance in accordance with the Medical Devices Regulation 2017\/745 with ad hoc notions on the structure of the surveillance system.<\/em><\/h6>\n<p><button id=\"rtec-form-toggle-button\" class=\"rtec-register-button rtec-form-toggle-button rtec-js-show\" style=\"display: inline-block;\" type=\"button\"><a class=\"link_register_eventi_esternamente\" href=\"https:\/\/www.eventbrite.it\/e\/biglietti-sorveglianza-post-commercializzazione-591169583137\" target=\"_blank\" rel=\"noopener\">Register<\/a><\/button><\/p>\n<h3>Webinar goals<\/h3>\n<p class=\"p1\">The webinar will provide an overview of post-market surveillance in accordance with the Medical Devices Regulation 2017\/745. The meeting will address issues such as:<\/p>\n<ul class=\"ul1\">\n<li class=\"li1\">definition of the surveillance system;<\/li>\n<li class=\"li1\">identification of documentation and key system-related activities;<\/li>\n<li class=\"li1\">obligations of economic operators.<\/li>\n<\/ul>\n<h3>Target group<\/h3>\n<p class=\"p1\">The webinar is aimed at everyone and is particularly suitable for Quality Assurance\/Regulatory Affairs of medical device manufacturers and contract medical device manufacturers.<\/p>\n<h3>What we learn from the webinar<\/h3>\n<p class=\"p1\">During the webinar will be provided notions on the structure of the surveillance system required by the Regulation.<\/p>\n<h3>Program<\/h3>\n<ul>\n<li>Definitions<\/li>\n<li>Timing of applicability<\/li>\n<li>Operators involved<\/li>\n<li>Documentation required by the Regulation<\/li>\n<\/ul>\n<h3>Lecturer<\/h3>\n<p class=\"p1\"><b>Irene Giovanetto<\/b>. Biomedical engineer, with a degree from the Polytechnic of Turin. Since 2019 he has been collaborating with <a href=\"https:\/\/biopmed.eu\/i-soci\/chemsafe-s-r-l\/\"><span class=\"s2\">Chemsafe S.r.l.<\/span><\/a> for regulatory advice on medical devices.<\/p>\n<p><button id=\"rtec-form-toggle-button\" class=\"rtec-register-button rtec-form-toggle-button rtec-js-show\" style=\"display: inline-block;\" type=\"button\"><a class=\"link_register_eventi_esternamente\" href=\"https:\/\/www.eventbrite.it\/e\/biglietti-sorveglianza-post-commercializzazione-591169583137\" target=\"_blank\" rel=\"noopener\">Register<\/a><\/button><\/p>\n","protected":false},"excerpt":{"rendered":"<p>A webinar that offers an overview of post-market surveillance in accordance with the Medical Devices Regulation 2017\/745 with ad hoc notions on the structure of the surveillance system. Register Webinar &hellip; <a href=\"https:\/\/biopmed.eu\/en\/evento-en\/post-marketing-surveillance\/\" class=\"more-link\">Continue reading <span class=\"screen-reader-text\">Post-marketing surveillance<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":10719,"template":"","meta":{"content-type":"","cybocfi_hide_featured_image":"","_tribe_events_status":"","_tribe_events_status_reason":"","footnotes":""},"tags":[],"tribe_events_cat":[141],"class_list":["post-11416","tribe_events","type-tribe_events","status-publish","has-post-thumbnail","hentry","tribe_events_cat-biopmed-events","cat_biopmed-events"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Post-marketing surveillance - bioPmed<\/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:\/\/biopmed.eu\/en\/evento-en\/post-marketing-surveillance\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Post-marketing surveillance - bioPmed\" \/>\n<meta property=\"og:description\" content=\"A webinar that offers an overview of post-market surveillance in accordance with the Medical Devices Regulation 2017\/745 with ad hoc notions on the structure of the surveillance system. 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