{"id":9592,"date":"2021-10-04T11:41:25","date_gmt":"2021-10-04T09:41:25","guid":{"rendered":"http:\/\/www.studioatatest.com\/bioindustry\/?p=9592"},"modified":"2021-10-04T12:06:56","modified_gmt":"2021-10-04T10:06:56","slug":"webinar_07-10-2021","status":"publish","type":"post","link":"http:\/\/www.studioatatest.com\/bioindustry\/2021\/10\/04\/webinar_07-10-2021\/?lang=en","title":{"rendered":"Webinar: Nuovo Regolamento Europeo per i Medical Devices MDR 745\/2017 &#8211; POST MARKET SURVEILLANCE"},"content":{"rendered":"[vc_row type=&#8221;in_container&#8221; full_screen_row_position=&#8221;middle&#8221; column_margin=&#8221;default&#8221; scene_position=&#8221;center&#8221; text_color=&#8221;dark&#8221; text_align=&#8221;left&#8221; overlay_strength=&#8221;0.3&#8243; shape_divider_position=&#8221;bottom&#8221; bg_image_animation=&#8221;none&#8221;][vc_column column_padding=&#8221;no-extra-padding&#8221; column_padding_position=&#8221;all&#8221; background_color_opacity=&#8221;1&#8243; background_hover_color_opacity=&#8221;1&#8243; column_link_target=&#8221;_self&#8221; column_shadow=&#8221;none&#8221; column_border_radius=&#8221;none&#8221; width=&#8221;1\/1&#8243; tablet_width_inherit=&#8221;default&#8221; tablet_text_alignment=&#8221;default&#8221; phone_text_alignment=&#8221;default&#8221; overlay_strength=&#8221;0.3&#8243; column_border_width=&#8221;none&#8221; column_border_style=&#8221;solid&#8221; bg_image_animation=&#8221;none&#8221;][image_with_animation image_url=&#8221;9593&#8243; alignment=&#8221;center&#8221; animation=&#8221;Fade In&#8221; hover_animation=&#8221;none&#8221; border_radius=&#8221;none&#8221; box_shadow=&#8221;none&#8221; image_loading=&#8221;default&#8221; max_width=&#8221;100%&#8221; max_width_mobile=&#8221;default&#8221;][vc_column_text]Gioved\u00ec 7 Ottobre alle ore 14:00, <a href=\"https:\/\/www.biopmed.eu\/\">bioPmed<\/a>, in collaborazione con <a href=\"https:\/\/www.biopmed.eu\/zc\/membri-biopmed.html?id=4154\">Flairnet<\/a> presenta il Webinar:<\/p>\n<p style=\"text-align: left;\">\u201cNuovo Regolamento Europeo per i Medical Devices &#8211; Post Market Surveillance\u201d<\/p>\n<div class=\"wpb_row vc_row vc_row-fluid\">\n<div class=\"vc_col-sm-12 wpb_column column_container\">\n<div class=\"event-item\">\n<p>Recentemente sono state riviste le direttive da seguire da parte dei produttori di Medical Device che operano nell\u2019Unione Europea nell\u2019ambito della \u2018Sorveglianza Post Market\u2019. In particolare, grazie al nuovo Regolamento (UE) 745\/2017 si passa ad una gestione dei dispositivi medici pi\u00f9 controllata e in termini legislativi da una direttiva (la MDD n.42 del 1993) ad un regolamento applicabile nei paesi dell\u2019Unione Europea.<\/p>\n<p>Il nuovo Regolamento 745\/2017:<\/p>\n<p>-Estende il campo di applicazione;<\/p>\n<p>-Fornisce maggior dettaglio sui diritti e doveri degli Operatori Economici;<\/p>\n<p>-Adegua le regole di classificazione e valutazione della conformit\u00e0 allo stato dell\u2019arte;<\/p>\n<p>-Richiede un processo proattivo per il monitoraggio delle attivit\u00e0 post-market;<\/p>\n<p>-Rafforza il sistema di vigilanza.<\/p>\n<p>A seguito del nuovo scenario, Flairnet ha realizzato l\u2019applicazione ConDOR PMS con l\u2019obiettivo di supportare i produttori nei processi di Sorveglianza Post Market (PMS) e nella \u2018compliance\u2019 al nuovo Regolamento 745\/2017.<\/p>\n<p>Ricordiamo che il webinar \u00e8 gratuito, scarica il<a href=\"http:\/\/www.studioatatest.com\/bioindustry\/wp-content\/uploads\/2021\/10\/VOLANTINO-PER-WEBINAR-7-OTTOBRE-Flairnet.pdf\"> programma<\/a> e iscriviti <a href=\"https:\/\/www.biopmed.eu\/zc\/evento.html?id=99\">qui<\/a><\/p>\n<\/div>\n<\/div>\n<\/div>\n[\/vc_column_text][\/vc_column][\/vc_row]\n","protected":false},"excerpt":{"rendered":"<p>[vc_row type=&#8221;in_container&#8221; 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