{"id":5394,"date":"2018-03-06T10:05:36","date_gmt":"2018-03-06T09:05:36","guid":{"rendered":"http:\/\/www.rapharm.eu\/en\/?p=5394"},"modified":"2018-03-27T11:04:26","modified_gmt":"2018-03-27T09:04:26","slug":"how-prepared-are-you-for-new-medical-devices-regulation","status":"publish","type":"post","link":"https:\/\/www.rapharm.eu\/en\/how-prepared-are-you-for-new-medical-devices-regulation\/","title":{"rendered":"Regulatory seminar: HOW PREPARED ARE YOU FOR NEW MEDICAL DEVICES REGULATION?"},"content":{"rendered":"<style type=\"text\/css\"><\/style><p><strong>10th May 2018<\/strong><br \/>\n<strong>Radisson Blu Plaza Hotel\u00a0Ljubljana (Slovenian language)<\/strong><\/p>\n<p><strong>Regulatory seminar:<br \/>\nHOW PREPARED ARE YOU FOR NEW<br \/>\nMEDICAL DEVICES REGULATION?<\/strong><\/p>\n<ul>\n<li><strong>5\u00a0steps to compliance<\/strong><\/li>\n<li><strong>\u201eGap\u201c analysis: How to prepare it?<\/strong><\/li>\n<li><strong><strong>From check list to\u00a0execution<\/strong><\/strong><\/li>\n<\/ul>\n<p>The new medical devices legislation has been adopted. And a third of the transition period has expired!<\/p>\n<p>The fundamental changes in legislation will affect all medical devices and all\u00a0stakeholders\u00a0dealing with them.\u00a0And this requires thorough preparation for implementation for all stakeholders, who wish to continue to trade with medical devices in future, since there is a lot of work and only a bit of time.<\/p>\n<p>Changes are not optional, changes are mandatory. Non-compliance will have serious consequences. Timely and appropriate planning is the key to success. So, let&#8217;s begin!<\/p>\n<p><strong>Click\u00a0<a href=\"http:\/\/www.rapharm.eu\/wp-content\/uploads\/2018\/03\/KakoStePripravljeniNaNovoZakonodajo_10052018-1.pdf\" target=\"_blank\">HERE<\/a>\u00a0for more information about the seminar.<\/strong><\/p>\n<p><strong>Click\u00a0<a href=\"http:\/\/www.rapharm.eu\/en\/apply-for-education\/\" target=\"_blank\">HERE<\/a>\u00a0to apply for the seminar.<\/strong><\/p>\n","protected":false},"excerpt":{"rendered":"<p>10th May 2018 Radisson Blu Plaza Hotel\u00a0Ljubljana (Slovenian language) Regulatory seminar: HOW PREPARED ARE YOU FOR NEW MEDICAL DEVICES REGULATION? 5\u00a0steps to compliance \u201eGap\u201c analysis: How to prepare it? From check list to\u00a0execution The new medical devices legislation has been adopted. And a third of the transition period has expired! The fundamental changes in legislation&#8230;<\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[40,39],"tags":[],"class_list":["post-5394","post","type-post","status-publish","format-standard","hentry","category-current-educations-and-trainings","category-regulatory-news"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v25.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Regulatory seminar: HOW PREPARED ARE YOU FOR NEW MEDICAL DEVICES REGULATION? - raPHARM<\/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:\/\/www.rapharm.eu\/kako-ste-pripravljeni-na-novo-zakonodajo-o-medicinskih-pripomockih\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Regulatory seminar: HOW PREPARED ARE YOU FOR NEW MEDICAL DEVICES REGULATION? - raPHARM\" \/>\n<meta property=\"og:description\" content=\"10th May 2018 Radisson Blu Plaza Hotel\u00a0Ljubljana (Slovenian language) Regulatory seminar: HOW PREPARED ARE YOU FOR NEW MEDICAL DEVICES REGULATION? 5\u00a0steps to compliance \u201eGap\u201c analysis: How to prepare it? 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