{"id":5681,"date":"2022-02-15T14:56:39","date_gmt":"2022-02-15T13:56:39","guid":{"rendered":"http:\/\/www.rapharm.eu\/en\/?p=5681"},"modified":"2022-02-15T15:31:12","modified_gmt":"2022-02-15T14:31:12","slug":"regulatory-online-workshop-medical-devices-compliance-check-medical-devices-prior-making-available-market","status":"publish","type":"post","link":"https:\/\/www.rapharm.eu\/en\/regulatory-online-workshop-medical-devices-compliance-check-medical-devices-prior-making-available-market\/","title":{"rendered":"Regulatory online workshop on medical devices: COMPLIANCE CHECK OF MEDICAL DEVICES PRIOR TO MAKING THEM AVAILABLE IN THE MARKET"},"content":{"rendered":"<style type=\"text\/css\"><\/style><p><strong>6th &amp; 7th April 2022<br \/>\n<\/strong><strong> Microsoft Teams\u00a0(Slovenian language)<\/strong><\/p>\n<p><strong>Regulatory online workshop on medical devices:<br \/>\nCOMPLIANCE CHECK OF MEDICAL DEVICES PRIOR TO MAKING THEM AVAILABLE IN THE MARKET<\/strong><\/p>\n<p>The workshop is intended for all economic operators (distributors, importers, authorized representatives, and manufacturers) involved in the supply chain of medical devices and who need practical skills for checking the compliance of requirements they need to check for devices before making them available in the market.<\/p>\n<p>The practical skills and the relevant templates will help you check whether the products in your portfolio are compliant with the Regulation (EU) 2017\/745, focusing on:<\/p>\n<ul>\n<li>their CE marking,<\/li>\n<li>the content of the EU Declaration of conformity of the device,<\/li>\n<li>the information provided with the device,<\/li>\n<li>information supplied by the importer and<\/li>\n<li>assigning a unique device identifier &#8211; UDI.<\/li>\n<\/ul>\n<p><strong>Click\u00a0<a href=\"https:\/\/www.rapharm.eu\/wp-content\/uploads\/2022\/02\/220406-07-MedPripDelavnicaDistributerji_Preverjanje.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">HERE<\/a>\u00a0for more information on the workshop.<\/strong><\/p>\n<p><strong>Click\u00a0<a href=\"http:\/\/www.rapharm.eu\/en\/apply-for-education\/\" target=\"_blank\" rel=\"noopener noreferrer\">HERE<\/a>\u00a0to apply for\u00a0the workshop.<\/strong><\/p>\n","protected":false},"excerpt":{"rendered":"<p>6th &amp; 7th April 2022 Microsoft Teams\u00a0(Slovenian language) Regulatory online workshop on medical devices: COMPLIANCE CHECK OF MEDICAL DEVICES PRIOR TO MAKING THEM AVAILABLE IN THE MARKET The workshop is intended for all economic operators (distributors, importers, authorized representatives, and manufacturers) involved in the supply chain of medical devices and who need practical skills for&#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-5681","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 - 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