{"id":11413,"date":"2023-02-14T22:27:30","date_gmt":"2023-02-14T21:27:30","guid":{"rendered":"https:\/\/biopmed.eu\/evento\/medical-devices-correct-handling-of-non-compliant-model\/"},"modified":"2023-02-14T22:27:30","modified_gmt":"2023-02-14T21:27:30","slug":"medical-devices-correct-handling-of-non-compliant-model","status":"publish","type":"tribe_events","link":"https:\/\/biopmed.eu\/en\/evento-en\/medical-devices-correct-handling-of-non-compliant-model\/","title":{"rendered":"Medical devices: correct handling of non-compliant model"},"content":{"rendered":"<h6><em>Starting from the general definition of non-conformity of a medical device, we will focus on how to manage a situation of this type, illustrating the process of managing the rework and\/or disposal phases.<\/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-dispositivi-medici-corretta-gestione-del-modello-non-conforme-547550156257\" target=\"_blank\" rel=\"noopener\">Register<\/a><\/button><\/p>\n<h3>Webinar goals<\/h3>\n<ul>\n<li>Understand the context of non-conformities within a Quality Management System<\/li>\n<li>Define the non-compliant product<\/li>\n<li>Internalize the flow of the non-conformity management process<\/li>\n<li>Describe the fate and disposal of a non-compliant product<\/li>\n<li>Define the concept of rework of a non-compliant product<\/li>\n<\/ul>\n<h3>Target group<\/h3>\n<p>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>The correct approach to dealing with non-compliant medical device cases<\/p>\n<h3>Program<\/h3>\n<ul>\n<li>General aspects<\/li>\n<li>Regulatory framework<\/li>\n<li>Control of a non-compliant product<\/li>\n<li>reworking<\/li>\n<\/ul>\n<h3>Lecturer<\/h3>\n<p><strong>Federica Carra<\/strong>. Graduated in Chemistry and Pharmaceutical Technology at the University of Turin, she has twenty years of experience in Pharmaceutical Quality Control, during which she obtained recognition for the suitability of a Qualified Person. Since 2016 he has been collaborating with Chemsafe for the design, Development and maintenance of ISO 9001 certification as Quality Manager and in the design and development of quality management systems for manufacturers of medical devices in accordance with current legislation. He is auditor of first and second part of Quality Management Systems GMP, ISO 9001, ISO 13485, ISO 22716, ISO 15378.<\/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-dispositivi-medici-corretta-gestione-del-modello-non-conforme-547550156257\" target=\"_blank\" rel=\"noopener\">Register<\/a><\/button><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Starting from the general definition of non-conformity of a medical device, we will focus on how to manage a situation of this type, illustrating the process of managing the rework &hellip; <a href=\"https:\/\/biopmed.eu\/en\/evento-en\/medical-devices-correct-handling-of-non-compliant-model\/\" class=\"more-link\">Continue reading <span class=\"screen-reader-text\">Medical devices: correct handling of non-compliant model<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":10670,"template":"","meta":{"content-type":"","cybocfi_hide_featured_image":"","_tribe_events_status":"","_tribe_events_status_reason":"","footnotes":""},"tags":[],"tribe_events_cat":[141],"class_list":["post-11413","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>Medical devices: correct handling of non-compliant model - 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\/medical-devices-correct-handling-of-non-compliant-model\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Medical devices: correct handling of non-compliant model - bioPmed\" \/>\n<meta property=\"og:description\" content=\"Starting from the general definition of non-conformity of a medical device, we will focus on how to manage a situation of this type, illustrating the process of managing the rework &hellip; 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