{"id":77070,"date":"2022-09-08T14:58:44","date_gmt":"2022-09-08T12:58:44","guid":{"rendered":"https:\/\/lightweb.dev\/s\/key2compliance\/?p=77070"},"modified":"2026-01-02T16:10:23","modified_gmt":"2026-01-02T15:10:23","slug":"meet-our-speakers-at-the-medical-device-product-life-cycle-conference","status":"publish","type":"post","link":"https:\/\/lightweb.dev\/s\/key2compliance\/events\/meet-our-speakers-at-the-medical-device-product-life-cycle-conference\/","title":{"rendered":"Meet our speakers at the Medical Device Product Life Cycle Conference!"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-post\" data-elementor-id=\"77070\" class=\"elementor elementor-77070\" data-elementor-post-type=\"post\">\n\t\t\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-3a7ddf00 elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"3a7ddf00\" data-element_type=\"section\" data-e-type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-6daf36d\" data-id=\"6daf36d\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-31933c4e elementor-widget elementor-widget-text-editor\" data-id=\"31933c4e\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p>We are excited and proud to have some of the most experienced speakers within the industry present at our <strong>Medical Device Product Life Cycle conference<\/strong> in Lund on the <strong>26-27th of October<\/strong>. Become inspired, get the latest knowledge, and turn your compliance strategies into a tool for success! Meet our speakers:<\/p><ul><li>Erik Hansson, Senior Expert in Global Harmonisation of Medical Device Regulations<br \/>Global trends within medical device regulations<\/li><li>Lena Cordie-Bancroft, Sector Lead for Medical Devices at\u00a0<a href=\"https:\/\/www.linkedin.com\/company\/bsi\/\" data-attribute-index=\"2\" data-entity-hovercard-id=\"urn:li:fs_miniCompany:162813\" data-entity-type=\"MINI_COMPANY\">BSI<\/a><br \/>Future-proof your device \u2013 How to manage changes in regulations and standards over the product life cycle<\/li><li>Judith de Wilde, Attorney at\u00a0<a href=\"https:\/\/www.linkedin.com\/company\/axon-lawyers\/\" data-attribute-index=\"6\" data-entity-hovercard-id=\"urn:li:fs_miniCompany:2255796\" data-entity-type=\"MINI_COMPANY\">Axon Lawyers<\/a><br \/>Interaction between manufacturers and other economic operators: How to effectively implement PMS in the supply chainMarketing &amp; Claims: How marketing, clinical evaluation and other MDR processes intertwine<\/li><li>Cyrille Michaud, Managing partner at\u00a0<a href=\"https:\/\/www.linkedin.com\/company\/md101-consulting\/\" data-attribute-index=\"10\" data-entity-hovercard-id=\"urn:li:fs_miniCompany:2700382\" data-entity-type=\"MINI_COMPANY\">MD101 Consulting<\/a><br \/>Device Software and Change control \u2013 how can SW manufacturers manage changes, under MDR?<\/li><li>Sofia Segersson, Owner, Consultant, Entrepeneur at Diabetesia<br \/>Medical Devices as Part of Your Daily Life \u2013 the User Perspective<\/li><li>Christoffer Ekstr\u00f6m, CEO at\u00a0<a href=\"https:\/\/www.linkedin.com\/company\/aimedicaltechnology\/\" data-attribute-index=\"16\" data-entity-hovercard-id=\"urn:li:fs_miniCompany:75133359\" data-entity-type=\"MINI_COMPANY\">AI Medical Technology<\/a><br \/>From user need to product specification \u2013 real world example<\/li><li>Ase Ek, Senior Consultant and Trainer at\u00a0<a href=\"https:\/\/www.linkedin.com\/company\/key2compliance%C2%AE\/\" data-attribute-index=\"20\" data-entity-hovercard-id=\"urn:li:fs_miniCompany:5086386\" data-entity-type=\"MINI_COMPANY\">Key2Compliance\u00ae<\/a><br \/>Being the \u2018Person Responsible for Regulatory Compliance\u2019 \u2013is this in fact a quality control, regulatory affairs, or both?<\/li><li>Josef Smeds, Managing Director at\u00a0<a href=\"https:\/\/www.linkedin.com\/company\/nordicinfu-care-ab\/\" data-attribute-index=\"24\" data-entity-hovercard-id=\"urn:li:fs_miniCompany:472623\" data-entity-type=\"MINI_COMPANY\">NordicInfu Care AB<\/a><br \/>How the industry work to meet both user needs, and expectations from the buyers<\/li><li>Jocelyn Akerberg, Global QA &amp; RA Manager at\u00a0<a href=\"https:\/\/www.linkedin.com\/company\/stille-ab\/\" data-attribute-index=\"28\" data-entity-hovercard-id=\"urn:li:fs_miniCompany:680590\" data-entity-type=\"MINI_COMPANY\">Stille AB<\/a><br \/>How Legal manufacturers shall control Contract manufacturers \u2013 the NB perspective<\/li><li>Jacques Thielen, Consultant Medical Devices at QRS<br \/>Post-Market Surveillance and Vigilance, and the links to Clinical Evaluation and Risk Management<\/li><li>Antti Virtanen, Solution Architect at\u00a0<a href=\"https:\/\/www.linkedin.com\/company\/innokas-medical\/\" data-attribute-index=\"34\" data-entity-hovercard-id=\"urn:li:fs_miniCompany:5013167\" data-entity-type=\"MINI_COMPANY\">Innokas Medical<\/a><br \/>Design transfer and contract manufacturing of medical devices \u2013 Practical tips and examples to mutually working relationship between customer and contract manufacturer<\/li><\/ul><p>\u00a0<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>We are excited and proud to have some of the most experienced speakers within the industry present at our Medical Device Product Life Cycle conference in Lund on the 26-27th of October. Become inspired, get the latest knowledge, and turn your compliance strategies into a tool for success! Meet our speakers: Erik Hansson, Senior Expert [&hellip;]<\/p>\n","protected":false},"author":18,"featured_media":77073,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"wds_primary_category":22,"footnotes":""},"categories":[22,21],"tags":[117,194,188],"blog-subject":[],"class_list":["post-77070","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-events","category-news","tag-medical-device","tag-quality-assurance","tag-regulatory-affairs"],"acf":[],"_links":{"self":[{"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/posts\/77070","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=77070"}],"version-history":[{"count":1,"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/posts\/77070\/revisions"}],"predecessor-version":[{"id":131863,"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/posts\/77070\/revisions\/131863"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/media\/77073"}],"wp:attachment":[{"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/media?parent=77070"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/categories?post=77070"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/tags?post=77070"},{"taxonomy":"blog-subject","embeddable":true,"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/blog-subject?post=77070"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}