{"id":6315,"date":"2023-11-09T10:04:54","date_gmt":"2023-11-09T09:04:54","guid":{"rendered":"https:\/\/www.rapharm.eu\/en\/?p=6315"},"modified":"2024-10-02T09:29:05","modified_gmt":"2024-10-02T07:29:05","slug":"redovna-edukacija-u-podrucju-regulatornih-medicinskih-proizvoda-ispunjavanje-obveza-za-uvoz-i-distribuciju-medicinskih-proizvoda","status":"publish","type":"post","link":"https:\/\/www.rapharm.eu\/en\/redovna-edukacija-u-podrucju-regulatornih-medicinskih-proizvoda-ispunjavanje-obveza-za-uvoz-i-distribuciju-medicinskih-proizvoda\/","title":{"rendered":"Regular training in the field of regulatory medical devices:  FULFILLMENT OF OBLIGATIONS FOR THE IMPORT AND DISTRIBUTION OF MEDICAL DEVICES"},"content":{"rendered":"<style type=\"text\/css\"><\/style>\n<p><strong>13th March 2024, Ljubljana<\/strong><\/p>\n\n\n\n<p><strong>Regular training in the field of regulatory medical devices:  <br>FULFILLMENT OF OBLIGATIONS FOR THE IMPORT AND DISTRIBUTION OF MEDICAL DEVICES <\/strong> <strong>(Slovenian language)<\/strong> <\/p>\n\n\n\n<p>Our regular\ntraining is aimed at those who want to gain basic knowledge, as well as those\nwho want to renew and upgrade their competences in the field of regulation for\nthe import and distribution of medical devices. This includes all personnel,\nfrom directors and management to salespeople and other employees involved in\nthe process of importing, distributing, or controlling the supply chain of\nmedical devices. If you are an importer, distributor, manufacturer of systems\nand packages (e.g., optics) or involved in the production of medical devices,\nthis training is essential to align and carry out your business in accordance\nwith the obligations imposed by the applicable legislation in this area.<\/p>\n\n\n\n<p>The training\nprogram includes:<\/p>\n\n\n\n<p>\u2022 basic knowledge\nof EU legislation related to medical devices;<\/p>\n\n\n\n<p>\u2022 practical\nguidelines for the import, wholesale and retail sale of medical devices;<\/p>\n\n\n\n<p>\u2022 proposals for\ndocumented procedures for managing the import and distribution of accessories;<\/p>\n\n\n\n<p>\u2022 useful tips for\nmaintaining the safety and performance of medical devices while you are in\ncharge.<\/p>\n\n\n\n<p>In addition, it is important to mention that the competent authorities requested proof of the suitability of the personnel to carry out activities in the field of import and distribution of medical devices. With the training, you will acquire the necessary knowledge and certificates that will satisfy this requirement of inspectors for the control of the market of medical devices.<\/p>\n\n\n\n<p><strong>Click\u00a0<a href=\"https:\/\/www.rapharm.eu\/wp-content\/uploads\/2024\/01\/240313-Informacije-Obveznosti-Uvoz_Distribucija.pdf\">HERE<\/a> for more information on the workshop.<\/strong><\/p>\n\n\n\n<p><strong>Click&nbsp;<a href=\"http:\/\/www.rapharm.eu\/en\/apply-for-education\/\" target=\"_blank\" rel=\"noreferrer noopener\">HERE<\/a>&nbsp;to apply for&nbsp;the workshop.<\/strong><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>13th March 2024, Ljubljana Regular training in the field of regulatory medical devices: FULFILLMENT OF OBLIGATIONS FOR THE IMPORT AND DISTRIBUTION OF MEDICAL DEVICES (Slovenian language) Our regular training is aimed at those who want to gain basic knowledge, as well as those who want to renew and upgrade their competences in the field of&#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],"tags":[],"class_list":["post-6315","post","type-post","status-publish","format-standard","hentry","category-current-educations-and-trainings"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v25.9 - 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