{"id":45735,"date":"2022-07-01T12:01:57","date_gmt":"2022-07-01T10:01:57","guid":{"rendered":"https:\/\/pharma-trend.com\/en\/supplier-management-with-the-new-medical-device-regulation-eu-mdr-745-2017-webinar-researchandmarkets-com\/"},"modified":"2022-07-01T12:01:57","modified_gmt":"2022-07-01T10:01:57","slug":"supplier-management-with-the-new-medical-device-regulation-eu-mdr-745-2017-webinar-researchandmarkets-com","status":"publish","type":"post","link":"https:\/\/pharma-trend.com\/en\/supplier-management-with-the-new-medical-device-regulation-eu-mdr-745-2017-webinar-researchandmarkets-com\/","title":{"rendered":"Supplier Management with the new Medical Device Regulation EU MDR 745\/2017 &#8211; Webinar &#8211; ResearchAndMarkets.com"},"content":{"rendered":"<div>\n<p>DUBLIN&#8211;(BUSINESS WIRE)&#8211;The <a target=\"_blank\" href=\"https:\/\/www.researchandmarkets.com\/reports\/4899728\/supplier-management-with-the-new-medical-device?utm_source=BW&amp;utm_medium=PressRelease&amp;utm_code=jm89gd&amp;utm_campaign=1720463+-+Supplier+Management+with+the+new+Medical+Device+Regulation+EU+MDR+745%2F2017+-+Webinar&amp;utm_exec=chdo54prd\" rel=\"nofollow noopener\" shape=\"rect\">&#8220;Supplier Management with the new Medical Device Regulation EU MDR 745\/2017&#8221;<\/a> webinar has been added to <strong>ResearchAndMarkets.com&#8217;s<\/strong> offering.\n<\/p>\n<p><a href=\"https:\/\/mms.businesswire.com\/media\/20220701005179\/en\/1503062\/4\/logo.jpg\"><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20220701005179\/en\/1503062\/21\/logo.jpg\"><\/a><\/p>\n<p>\nThe new medical device regulation EU MDR 745\/2017 in the European Union has a lot of new requirements. One hot topic is the focus on the supply chain and the interfaces to the EN ISO 13485:2016.\n<\/p>\n<p>\nBoth, the ISO standard and the MDR requires for outsourced processes additional activities and be careful with outsourced processes. Those are not only on the classic supplier side. Those are also on the other side of the company in the area of sales and post market activities. The understanding of this changes and how to implement is essential to keep your certificates.\n<\/p>\n<p>\nYou should attend this webinar to understand, what are the changes to the previous medical device regulation and how to implement the changes in your current quality management system in a simple and quick way. Your implementation need smart ideas to reach the right level to pass the quality management audit by your certification company or notified body.\n<\/p>\n<p>\n<strong>The webinar will describe the following vital topics:<\/strong>\n<\/p>\n<ul>\n<li>\nIntroduction, who must apply the new EU MDR 745\/2017 requirements\n<\/li>\n<li>\nOverview about the changes of the EU MDR 745\/2017 regarding supplier and outsourced activities.\n<\/li>\n<li>\nExplaining of each change\n<\/li>\n<li>\nSmart and fast ways to implement the changes in your quality management system\n<\/li>\n<li>\nFast track internal audit to approve the changes\n<\/li>\n<li>\nWho is responsible for the activities?\n<\/li>\n<li>\nWhich (new) roles in the company required?\n<\/li>\n<\/ul>\n<p>\n<strong>Who Should Attend:<\/strong>\n<\/p>\n<p>\nCEO&#8217;s, purchasing manager, quality\/regulatory affairs manager, quality representatives of medical device manufacturers, importers, distributors, and dealers who work with European Union, European Economic Area, Switzerland, Turkey\n<\/p>\n<p>\n<strong>Key Topics Covered:<\/strong>\n<\/p>\n<ul>\n<li>\nCloser regulatory binding of the ISO to the new EU MDR\n<\/li>\n<li>\nResponsibilities for outsourced processes\n<\/li>\n<li>\nWhat are outsourced processes?\n<\/li>\n<li>\nAdjustments in the management review\n<\/li>\n<li>\nAdjustments in the audit process\n<\/li>\n<li>\nHow to onboard the supplier?\n<\/li>\n<li>\nExamples from outsourced R&amp;D-, manufacturing-, lab-test &#8211; processes\n<\/li>\n<li>\nExamples from outsourced sales processes\n<\/li>\n<\/ul>\n<p>\nFor more information about this webinar visit <a target=\"_blank\" href=\"https:\/\/www.researchandmarkets.com\/reports\/4899728\/supplier-management-with-the-new-medical-device?utm_source=BW&amp;utm_medium=PressRelease&amp;utm_code=jm89gd&amp;utm_campaign=1720463+-+Supplier+Management+with+the+new+Medical+Device+Regulation+EU+MDR+745%2F2017+-+Webinar&amp;utm_exec=chdo54prd\" rel=\"nofollow noopener\" shape=\"rect\">https:\/\/www.researchandmarkets.com\/r\/75wu1m<\/a>\n<\/p>\n<p> <b>Contacts<\/b> <\/p>\n<p>\nResearchAndMarkets.com<br \/>\n<br \/>Laura Wood, Senior Press Manager<br \/>\n<br \/><a target=\"_blank\" href=\"m&#97;&#105;&#x6c;&#x74;&#x6f;&#x3a;p&#114;&#101;&#115;&#x73;&#x40;&#x72;es&#101;&#97;&#x72;&#x63;&#x68;an&#100;&#109;&#x61;&#x72;&#x6b;et&#115;&#46;&#x63;&#x6f;&#x6d;\" rel=\"nofollow noopener\" shape=\"rect\">&#x70;&#x72;&#x65;&#x73;&#115;&#64;&#114;es&#x65;&#x61;&#x72;&#x63;&#x68;&#97;&#110;&#100;ma&#x72;&#x6b;&#x65;&#x74;&#x73;&#46;&#99;&#111;m<\/a><br \/>For E.S.T Office Hours Call 1-917-300-0470<br \/>\n<br \/>For U.S.\/CAN Toll Free Call 1-800-526-8630<br \/>\n<br \/>For GMT Office Hours Call +353-1-416-8900\n<\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>DUBLIN&#8211;(BUSINESS WIRE)&#8211;The &#8220;Supplier Management with the new Medical Device Regulation EU MDR 745\/2017&#8221; webinar has been added to ResearchAndMarkets.com&#8217;s offering. The new medical device regulation EU MDR 745\/2017 in the European Union has a lot of new requirements. One hot topic is the focus on the supply chain and the interfaces to the EN ISO &#8230; <span class=\"more\"><a class=\"more-link\" href=\"https:\/\/pharma-trend.com\/en\/supplier-management-with-the-new-medical-device-regulation-eu-mdr-745-2017-webinar-researchandmarkets-com\/\">[Read more&#8230;]<\/a><\/span><\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[13],"tags":[],"class_list":{"0":"entry","1":"post","2":"publish","3":"author-business","4":"post-45735","6":"format-standard","7":"category-industry"},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Supplier Management with the new Medical Device Regulation EU MDR 745\/2017 - Webinar - ResearchAndMarkets.com - Pharma Trend<\/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:\/\/pharma-trend.com\/en\/supplier-management-with-the-new-medical-device-regulation-eu-mdr-745-2017-webinar-researchandmarkets-com\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Supplier Management with the new Medical Device Regulation EU MDR 745\/2017 - Webinar - ResearchAndMarkets.com - Pharma Trend\" \/>\n<meta property=\"og:description\" content=\"DUBLIN&#8211;(BUSINESS WIRE)&#8211;The &#8220;Supplier Management with the new Medical Device Regulation EU MDR 745\/2017&#8221; webinar has been added to ResearchAndMarkets.com&#8217;s offering. 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