{"id":58643,"date":"2019-01-22T14:00:24","date_gmt":"2019-01-22T12:00:24","guid":{"rendered":"https:\/\/www.tehnopol.ee\/?p=58643"},"modified":"2023-11-08T20:40:36","modified_gmt":"2023-11-08T18:40:36","slug":"medical-device-regulation-workshop","status":"publish","type":"post","link":"https:\/\/www.tehnopol.ee\/en\/medical-device-regulation-workshop\/","title":{"rendered":"Last chance! Connected Health Cluster workshop: Medical Device Regulation"},"content":{"rendered":"<p><a href=\"https:\/\/www.tehnopol.ee\/en\/medical-device-regulation-workshop\/mdr-workshop\/\" rel=\"attachment wp-att-58833\"><img decoding=\"async\" class=\"alignleft size-full wp-image-58833\" src=\"https:\/\/www.tehnopol.ee\/wp-content\/uploads\/2019\/01\/MDR-workshop.png\" alt=\"\" width=\"960\" height=\"540\" srcset=\"https:\/\/www.tehnopol.ee\/wp-content\/uploads\/2019\/01\/MDR-workshop.png 960w, https:\/\/www.tehnopol.ee\/wp-content\/uploads\/2019\/01\/MDR-workshop-600x338.png 600w, https:\/\/www.tehnopol.ee\/wp-content\/uploads\/2019\/01\/MDR-workshop-300x169.png 300w, https:\/\/www.tehnopol.ee\/wp-content\/uploads\/2019\/01\/MDR-workshop-768x432.png 768w, https:\/\/www.tehnopol.ee\/wp-content\/uploads\/2019\/01\/MDR-workshop-400x225.png 400w, https:\/\/www.tehnopol.ee\/wp-content\/uploads\/2019\/01\/MDR-workshop-200x113.png 200w\" sizes=\"(max-width: 960px) 100vw, 960px\"><\/a><\/p>\n<p style=\"text-align: justify;\"><strong>Connected Health Cluster is organizing a\u00a0<\/strong><strong>Medical Device Regulation\u00a0<\/strong><strong>workshop\u00a0 on the 31st of January at 10:00-13:00.<\/strong><\/p>\n<p style=\"text-align: justify;\"><strong>The seminar will answer the questions:<\/strong><\/p>\n<ul style=\"text-align: justify;\">\n<li>What is a medical device? How to get medical devices through regulatory audits? What does the new MDR require?<\/li>\n<li>What is an ISO 13485 compliant Quality Management System and who needs it?<\/li>\n<li>Who is required to have ISO 14971 compliant risk management and IEC 62304 compliant software development in place?<\/li>\n<li>How to kickstart regulatory compliance with Jira and Confluence add-ons?<\/li>\n<\/ul>\n<p style=\"text-align: justify;\"><strong>Agenda:<\/strong><\/p>\n<p style=\"text-align: justify;\">9:30-10:00 Welcome Coffee, registration<\/p>\n<p style=\"text-align: justify;\">10:00-11:15 Medical Device Regulation: What are changes in reality?<\/p>\n<p style=\"text-align: justify;\">speaker Mr. Jani Hopia, Senior Regulatory Specialist from Kasve Ltd<\/p>\n<p style=\"text-align: justify;\">11:15-11:30 Coffee and networking<\/p>\n<p style=\"text-align: justify;\">11:30-12:45 Medical Device Regulatory Compliance on Jira &amp; Confluence with SoftComply, speaker Mr. Margus Nael, Co-Founder &amp; CTO of SoftComply<\/p>\n<p style=\"text-align: justify;\">Place: Tallinn Science Park Tehnopol, Teaduspargi 6\/1, seminar room Merkuur<\/p>\n<p style=\"text-align: justify;\">Language: English<\/p>\n<p style=\"text-align: justify;\">Fee: Free of charge for CHC and Tehnopol partners. Others 50,00 EUR + VAT<\/p>\n<p style=\"text-align: justify;\">Target group: Connected Health Cluster members, also all other software developers who provide software solutions to medical device manufacturers. Registration is\u00a0<a href=\"https:\/\/docs.google.com\/forms\/d\/e\/1FAIpQLSf8LaerxBFjC9hFBLJQ93erfErFFVVK7KG6guFJOvS4EWxj2Q\/viewform\"><strong>here<\/strong>.<\/a> Please register<strong> before<\/strong> <strong>25.01.2019.<\/strong>\u00a0More information <a href=\"mailto:Piret.hirv@tehnopol.ee\">Piret.hirv@tehnopol.ee<\/a><\/p>\n<p><a href=\"https:\/\/www.facebook.com\/events\/963584300504574\/\">See also Facebook event here.<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Connected Health Cluster is organizing a\u00a0Medical Device Regulation\u00a0workshop\u00a0 on the 31st of January at 10:00-13:00. The seminar will answer the questions: What is a medical device? How to get medical devices through regulatory audits? What does the new MDR require? What is an ISO 13485 compliant Quality Management System and who needs it? Who is [&hellip;]<\/p>\n","protected":false},"author":26,"featured_media":58833,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"inline_featured_image":false,"_s2mail":"yes","footnotes":""},"categories":[17],"tags":[],"class_list":["post-58643","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-uncategorized"],"acf":[],"_links":{"self":[{"href":"https:\/\/www.tehnopol.ee\/en\/wp-json\/wp\/v2\/posts\/58643","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.tehnopol.ee\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.tehnopol.ee\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.tehnopol.ee\/en\/wp-json\/wp\/v2\/users\/26"}],"replies":[{"embeddable":true,"href":"https:\/\/www.tehnopol.ee\/en\/wp-json\/wp\/v2\/comments?post=58643"}],"version-history":[{"count":3,"href":"https:\/\/www.tehnopol.ee\/en\/wp-json\/wp\/v2\/posts\/58643\/revisions"}],"predecessor-version":[{"id":147518,"href":"https:\/\/www.tehnopol.ee\/en\/wp-json\/wp\/v2\/posts\/58643\/revisions\/147518"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.tehnopol.ee\/en\/wp-json\/wp\/v2\/media\/58833"}],"wp:attachment":[{"href":"https:\/\/www.tehnopol.ee\/en\/wp-json\/wp\/v2\/media?parent=58643"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.tehnopol.ee\/en\/wp-json\/wp\/v2\/categories?post=58643"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.tehnopol.ee\/en\/wp-json\/wp\/v2\/tags?post=58643"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}