{"id":3925,"date":"2021-10-04T12:22:45","date_gmt":"2021-10-04T10:22:45","guid":{"rendered":"https:\/\/www.universalmedica.com\/webinar-materiovigilance-everything-you-need-to-know-about-the-new-european-regulation-on-medical-devices-eu-regulation-2017-745-2\/"},"modified":"2025-05-23T11:24:07","modified_gmt":"2025-05-23T09:24:07","slug":"webinar-materiovigilance-everything-you-need-to-know-about-the-new-european-regulation-on-medical-devices-eu-regulation-2017-745-2","status":"publish","type":"post","link":"https:\/\/www.universalmedica.com\/en\/webinar-materiovigilance-everything-you-need-to-know-about-the-new-european-regulation-on-medical-devices-eu-regulation-2017-745-2\/","title":{"rendered":"Webinar &#8211; Materiovigilance: Everything you need to know about the new European Regulation on Medical Devices (EU Regulation 2017\/745)"},"content":{"rendered":"<p><strong>Language<\/strong> \u2013 French<\/p>\n<p>This webinar aims to provide clarification on the new EU Regulation on medical devices (EU Regulation 2017\/745) which came into force on 25 May 2021.<\/p>\n<p>The new regulation outlines a more robust classification system for medical devices and sets out specific requirements for manufacturers, importers, and distributors of medical devices.<\/p>\n<p>This webinar will focus on the new EU regulation on post-marketing surveillance of medical devices and will address the following issues:<\/p>\n<p>&#8211; How to set up post-market surveillance of medical devices and which data to monitor?<\/p>\n<p>&#8211; How does incident reporting work?<\/p>\n<p>&#8211; What are the periodic reports to be written, for what purpose and what do they contain?<\/p>\n<p>&#8211; How to set up a risk management plan?<\/p>\n<p>At the end of the webinar, you will have the opportunity to ask our experts any questions you may have.<\/p>\n<p>Register now\u00a0<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Language \u2013 French This webinar aims to provide clarification on the new EU Regulation on medical devices (EU Regulation 2017\/745) which came into force on 25 May 2021. The new regulation outlines a more robust classification system for medical devices and sets out specific requirements for manufacturers, importers, and distributors of medical devices. 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