We are beginning our countdown until our Medical Device Product Life Cycle Conference on October 26-27th! We are thrilled to see how many of you have signed up to join us. There are still some spaces left. If you haven\u2019t yet registered, but are thinking about doing so, we encourage you to REGISTER NOW to secure your spot!<\/p>\n
This must-attend conference will broaden your understanding, give you new skills and expand your professional network. Our 2-day conference will be full of presentations, interactions, and workshops that will give new insights into the latest tools and interpretation of the latest rules and regulations. But most of all, listen and learn from some of the most experienced experts within the industry!<\/p>\n
Erik Hansson, Senior Expert in Global Harmonisation of Medical Device Regulations<\/strong> Emma Glass, University Partnerships Manager, Healthcare Technologies at BSI<\/strong> Cyrille Michaud, Managing <\/strong>P<\/strong>artner at MD101 Consulting<\/strong> Christoffer Ekstr\u00f6m, CEO at AI Medical Technology Judith de Wilde, Attorney at Axon Lawyers<\/strong> – Marketing & Claims: How marketing, clinical evaluation and other MDR processes intertwine<\/p>\n Sofia Segersson, Owner, Consultant, Entrepeneur at Diabetesia<\/strong> \u00c5se Ek, Senior Consultant and Trainer at Key2Compliance<\/strong> Josef Smeds, Managing Director, NordicInfu Care Jocelyn \u00c5kerberg<\/strong>, Global QA & RA Manager, Stille Antti Virtanen, Solution Architect at Innokas Medical<\/strong> Jacques Thielen, Consultant Medical Devices at QRS Please, don\u2019t miss out on this opportunity to join our upcoming two-day! Register now!<\/p>\n We hope to meet you in Lund!<\/p>\n","protected":false},"excerpt":{"rendered":" We are beginning our countdown until our Medical Device Product Life Cycle Conference on October 26-27th! We are thrilled to see how many of you have signed up to join us. There are still some spaces left. If you haven\u2019t yet registered, but are thinking about doing so, we encourage you to REGISTER NOW to […]<\/p>\n","protected":false},"author":18,"featured_media":78243,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"wds_primary_category":22,"footnotes":""},"categories":[22,21],"tags":[117,188],"blog-subject":[],"class_list":["post-78239","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-events","category-news","tag-medical-device","tag-regulatory-affairs"],"acf":[],"_links":{"self":[{"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/posts\/78239","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/users\/18"}],"replies":[{"embeddable":true,"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/comments?post=78239"}],"version-history":[{"count":0,"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/posts\/78239\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/media\/78243"}],"wp:attachment":[{"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/media?parent=78239"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/categories?post=78239"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/tags?post=78239"},{"taxonomy":"blog-subject","embeddable":true,"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/blog-subject?post=78239"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
\n<\/strong>– Global trends within medical device regulations<\/p>\n
\n– <\/strong>Future-proof your device \u2013 How to manage changes in regulations and standards over the product life cycle<\/p>\n
\n<\/strong>– <\/strong>Cybersecurity: How to deal with it throughout the Medical Device lifecycle?<\/p>\n
\n<\/strong>– <\/strong>From user need to product specification \u2013 real world example<\/p>\n
\n– Interaction between manufacturers and other economic operators: How to effectively implement PMS in the supply chain<\/p>\n
\n– Medical Devices as Part of Your Daily Life \u2013 the User Perspective<\/p>\n
\n– Being the \u2018Person Responsible for Regulatory Compliance\u2019 \u2013is this in fact a quality control, regulatory affairs, or both?<\/p>\n
\n<\/strong>– <\/strong>How the industry work to meet both user needs, and expectations from the buyers<\/p>\n
\n– <\/strong>How Legal manufacturers shall control Contract manufacturers \u2013 the NB perspective<\/p>\n
\n– Design transfer and contract manufacturing of medical devices \u2013 Practical tips and examples to mutually working relationship between customer and contract manufacturer<\/p>\n
\n<\/strong>– <\/strong>Post-Market Surveillance and Vigilance, and the links to Clinical Evaluation and Risk Management<\/p>\n