{"id":5455,"date":"2018-09-25T11:28:23","date_gmt":"2018-09-25T09:28:23","guid":{"rendered":"http:\/\/www.rapharm.eu\/en\/?p=5455"},"modified":"2018-10-19T10:33:28","modified_gmt":"2018-10-19T08:33:28","slug":"new-liabilities-and-responsibilities-of-distributors-of-medical-devices-in-the-eu","status":"publish","type":"post","link":"https:\/\/www.rapharm.eu\/en\/new-liabilities-and-responsibilities-of-distributors-of-medical-devices-in-the-eu\/","title":{"rendered":"Regulatory seminar and workshop on medical devices: NEW LIABILITIES AND RESPONSIBILITIES OF DISTRIBUTORS OF MEDICAL DEVICES IN THE EU &#8211; Why to review current agreements?"},"content":{"rendered":"<style type=\"text\/css\"><\/style><p><strong>27th &amp; 28th November 2018<\/strong><br \/>\n<strong>Radisson Blu Plaza Hotel\u00a0Ljubljana (Slovenian language)<\/strong><\/p>\n<p><strong>Regulatory seminar and workshop on medical devices<br \/>\n<\/strong><strong>NEW LIABILITIES AND RESPONSIBILITIES OF DISTRIBUTORS OF MEDICAL DEVICES IN THE EU &#8211; Why to review current agreements?<br \/>\n<\/strong><\/p>\n<p>The new legislation on medical devices is adopted, and the transitional period for its implementation is slowly running out. Distributors of medical devices will have to harmonize their business with new requirements. Therefore, it is necessary not only to become acquainted with changes and their potential impact on business, but also to prevent surprises in practice due to overlooked details, different interpretation of requirements or methods of their fulfillment. Sometimes this is an existential importance for the company. In particular, it is a sensitive area of a new division of responsibility in relation to manufacturers of medical devices, authorized representatives, importers or users.<br \/>\nThe seminar and the workshop are originally intended for distributors of medical devices, but they are suitable and useful for all other business entities as well, since the changes also affect their business.<\/p>\n<p><strong>Click\u00a0<a href=\"http:\/\/www.rapharm.eu\/wp-content\/uploads\/2018\/09\/SeminarDelavnicaDistributerji2728112018-1.pdf\" target=\"_blank\">HERE<\/a>\u00a0for more information about seminar and workshop.<\/strong><\/p>\n<p><strong>Click\u00a0<a href=\"http:\/\/www.rapharm.eu\/en\/apply-for-education\/\" target=\"_blank\">HERE<\/a>\u00a0to apply for seminar and workshop.<\/strong><\/p>\n","protected":false},"excerpt":{"rendered":"<p>27th &amp; 28th November 2018 Radisson Blu Plaza Hotel\u00a0Ljubljana (Slovenian language) Regulatory seminar and workshop on medical devices NEW LIABILITIES AND RESPONSIBILITIES OF DISTRIBUTORS OF MEDICAL DEVICES IN THE EU &#8211; Why to review current agreements? The new legislation on medical devices is adopted, and the transitional period for its implementation is slowly running out&#8230;.<\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[40,39,30],"tags":[],"class_list":["post-5455","post","type-post","status-publish","format-standard","hentry","category-current-educations-and-trainings","category-regulatory-news","category-uncategorized"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v25.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Regulatory seminar and workshop on medical devices: NEW LIABILITIES AND RESPONSIBILITIES OF DISTRIBUTORS OF MEDICAL DEVICES IN THE EU - Why to review current agreements? - 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\/nove-obveznosti-in-odgovornosti-distributerjev-medicinskih-pripomockov\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Regulatory seminar and workshop on medical devices: NEW LIABILITIES AND RESPONSIBILITIES OF DISTRIBUTORS OF MEDICAL DEVICES IN THE EU - Why to review current agreements? - raPHARM\" \/>\n<meta property=\"og:description\" content=\"27th &amp; 28th November 2018 Radisson Blu Plaza Hotel\u00a0Ljubljana (Slovenian language) Regulatory seminar and workshop on medical devices NEW LIABILITIES AND RESPONSIBILITIES OF DISTRIBUTORS OF MEDICAL DEVICES IN THE EU &#8211; Why to review current agreements? The new legislation on medical devices is adopted, and the transitional period for its implementation is slowly running out....\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.rapharm.eu\/nove-obveznosti-in-odgovornosti-distributerjev-medicinskih-pripomockov\/\" \/>\n<meta property=\"og:site_name\" content=\"raPHARM\" \/>\n<meta property=\"article:published_time\" content=\"2018-09-25T09:28:23+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2018-10-19T08:33:28+00:00\" \/>\n<meta name=\"author\" content=\"rapharm\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"rapharm\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/www.rapharm.eu\/nove-obveznosti-in-odgovornosti-distributerjev-medicinskih-pripomockov\/\",\"url\":\"https:\/\/www.rapharm.eu\/nove-obveznosti-in-odgovornosti-distributerjev-medicinskih-pripomockov\/\",\"name\":\"Regulatory seminar and workshop on medical devices: NEW LIABILITIES AND RESPONSIBILITIES OF DISTRIBUTORS OF MEDICAL DEVICES IN THE EU - Why to review current agreements? - raPHARM\",\"isPartOf\":{\"@id\":\"https:\/\/www.rapharm.eu\/#website\"},\"datePublished\":\"2018-09-25T09:28:23+00:00\",\"dateModified\":\"2018-10-19T08:33:28+00:00\",\"author\":{\"@id\":\"https:\/\/www.rapharm.eu\/#\/schema\/person\/ba2051c1c51d2328945ac838b3f1d7e1\"},\"breadcrumb\":{\"@id\":\"https:\/\/www.rapharm.eu\/nove-obveznosti-in-odgovornosti-distributerjev-medicinskih-pripomockov\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/www.rapharm.eu\/nove-obveznosti-in-odgovornosti-distributerjev-medicinskih-pripomockov\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/www.rapharm.eu\/nove-obveznosti-in-odgovornosti-distributerjev-medicinskih-pripomockov\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\/\/www.rapharm.eu\/en\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Regulatory seminar and workshop on medical devices: NEW LIABILITIES AND RESPONSIBILITIES OF DISTRIBUTORS OF MEDICAL DEVICES IN THE EU &#8211; Why to review current agreements?\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/www.rapharm.eu\/#website\",\"url\":\"https:\/\/www.rapharm.eu\/\",\"name\":\"raPHARM\",\"description\":\"Just another WordPress site\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/www.rapharm.eu\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"},{\"@type\":\"Person\",\"@id\":\"https:\/\/www.rapharm.eu\/#\/schema\/person\/ba2051c1c51d2328945ac838b3f1d7e1\",\"name\":\"rapharm\",\"image\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\/\/www.rapharm.eu\/#\/schema\/person\/image\/\",\"url\":\"https:\/\/secure.gravatar.com\/avatar\/9ea8e299db6979b3c68307fd37c34f245020d4996bcf2ccdeec4bce3350fcc24?s=96&d=mm&r=g\",\"contentUrl\":\"https:\/\/secure.gravatar.com\/avatar\/9ea8e299db6979b3c68307fd37c34f245020d4996bcf2ccdeec4bce3350fcc24?s=96&d=mm&r=g\",\"caption\":\"rapharm\"},\"url\":\"https:\/\/www.rapharm.eu\/en\/author\/rapharm\/\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Regulatory seminar and workshop on medical devices: NEW LIABILITIES AND RESPONSIBILITIES OF DISTRIBUTORS OF MEDICAL DEVICES IN THE EU - Why to review current agreements? - raPHARM","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.rapharm.eu\/nove-obveznosti-in-odgovornosti-distributerjev-medicinskih-pripomockov\/","og_locale":"en_US","og_type":"article","og_title":"Regulatory seminar and workshop on medical devices: NEW LIABILITIES AND RESPONSIBILITIES OF DISTRIBUTORS OF MEDICAL DEVICES IN THE EU - Why to review current agreements? - raPHARM","og_description":"27th &amp; 28th November 2018 Radisson Blu Plaza Hotel\u00a0Ljubljana (Slovenian language) Regulatory seminar and workshop on medical devices NEW LIABILITIES AND RESPONSIBILITIES OF DISTRIBUTORS OF MEDICAL DEVICES IN THE EU &#8211; Why to review current agreements? 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