{"id":5496,"date":"2019-03-25T20:46:37","date_gmt":"2019-03-25T19:46:37","guid":{"rendered":"http:\/\/www.rapharm.eu\/en\/2019\/03\/25\/priprava-dokumentiranih-postopkov-za-izpolnitev-zahtev-nove-zakonodaje-na-podrocju-medicinskih-pripomockov\/"},"modified":"2020-02-21T18:34:39","modified_gmt":"2020-02-21T17:34:39","slug":"preparation-of-documented-procedures-for-meeting-the-requirements-of-the-new-regulation-in-the-field-of-distribution-of-medical-devices","status":"publish","type":"post","link":"https:\/\/www.rapharm.eu\/en\/preparation-of-documented-procedures-for-meeting-the-requirements-of-the-new-regulation-in-the-field-of-distribution-of-medical-devices\/","title":{"rendered":"Regulatory workshop: PREPARATION OF DOCUMENTED PROCEDURES FOR MEETING THE REQUIREMENTS OF THE NEW REGULATION IN THE FIELD OF DISTRIBUTION OF MEDICAL DEVICES"},"content":{"rendered":"<style type=\"text\/css\"><\/style><p><strong>Additional\u00a0term:\u00a0Date to be determined<\/strong><br \/>\n<strong>raPHARM premises, Miklo\u0161i\u010deva 30,\u00a0Ljubljana (Slovenian language)<\/strong><\/p>\n<p><strong>Regulatory workshop<br \/>\nPREPARATION OF DOCUMENTED PROCEDURES FOR MEETING THE REQUIREMENTS OF THE NEW REGULATION IN THE FIELD OF DISTRIBUTION OF MEDICAL DEVICES<br \/>\n<\/strong><\/p>\n<p>The workshop is intended for all economic operators (distributors, sellers, importers, authorized representatives and manufacturers) of medical devices included in the supply chain of medical devices that need practical knowledge of distributors&#8217; obligations as described in the new regulation, together with additional guidelines and approaches, which can be used to fulfill these obligations.<\/p>\n<p>The acquired practical knowledge and appropriate proposals for the gap analysis, process inventory (OP\/SOP) and the keeping of records that you receive will help you identify, adapt and\/or establish appropriate procedures in accordance with the new legislation, suitable for your business mode and medical devices class.<\/p>\n<p><strong>Click\u00a0<a href=\"http:\/\/www.rapharm.eu\/wp-content\/uploads\/2019\/03\/MedPripDelavnicaDistributerji_Uredbe-9.pdf\" target=\"_blank\">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\">HERE<\/a>\u00a0to apply for the workshop.<\/strong><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Additional\u00a0term:\u00a0Date to be determined raPHARM premises, Miklo\u0161i\u010deva 30,\u00a0Ljubljana (Slovenian language) Regulatory workshop PREPARATION OF DOCUMENTED PROCEDURES FOR MEETING THE REQUIREMENTS OF THE NEW REGULATION IN THE FIELD OF DISTRIBUTION OF MEDICAL DEVICES The workshop is intended for all economic operators (distributors, sellers, importers, authorized representatives and manufacturers) of medical devices included in the supply chain&#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-5496","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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