{"id":75961,"date":"2022-06-07T16:48:29","date_gmt":"2022-06-07T14:48:29","guid":{"rendered":"https:\/\/lightweb.dev\/s\/key2compliance\/?p=75961"},"modified":"2026-01-02T16:12:17","modified_gmt":"2026-01-02T15:12:17","slug":"first-speaker-announced-medical-device-product-life-cycle","status":"publish","type":"post","link":"https:\/\/lightweb.dev\/s\/key2compliance\/events\/first-speaker-announced-medical-device-product-life-cycle\/","title":{"rendered":"First speaker announced – Medical Device Product Life Cycle Conference"},"content":{"rendered":"

Make compliance your success factor –\u00a0 a conference for QA\/RA professionals<\/h2>\n

We are delighted to introduce the first speaker Cyrille Michaud<\/strong><\/a> at our upcoming conference on the 26-27th of Ocotober in Lund, Sweden<\/strong>.<\/p>\n

The title of Cyrille\u2019s presentation is \u201cDevice Software and Change control – how can SW manufacturers manage changes under MDR?\u201d\u00a0<\/strong><\/p>\n

Short introduction to Cyrille’s presentation:<\/p>\n

Making changes to software design usually takes short periods of time, compared to hardware medical devices. Manufacturers have to reconcile the pace of design changes in software with the slower pace of regulatory approvals. In this presentation I will clarify how these requirements apply to SW and provide some tools for how to address this challenge Looking forward to seeing you in the audience!<\/p>\n","protected":false},"excerpt":{"rendered":"

Make compliance your success factor –\u00a0 a conference for QA\/RA professionals We are delighted to introduce the first speaker Cyrille Michaud at our upcoming conference on the 26-27th of Ocotober in Lund, Sweden. The title of Cyrille\u2019s presentation is \u201cDevice Software and Change control – how can SW manufacturers manage changes under MDR?\u201d\u00a0 Short introduction […]<\/p>\n","protected":false},"author":18,"featured_media":1004,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"wds_primary_category":22,"footnotes":""},"categories":[22,21],"tags":[186,194,188],"blog-subject":[],"class_list":["post-75961","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-events","category-news","tag-medical-devices","tag-quality-assurance","tag-regulatory-affairs"],"acf":[],"_links":{"self":[{"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/posts\/75961","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=75961"}],"version-history":[{"count":1,"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/posts\/75961\/revisions"}],"predecessor-version":[{"id":131865,"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/posts\/75961\/revisions\/131865"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/media\/1004"}],"wp:attachment":[{"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/media?parent=75961"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/categories?post=75961"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/tags?post=75961"},{"taxonomy":"blog-subject","embeddable":true,"href":"https:\/\/lightweb.dev\/s\/key2compliance\/wp-json\/wp\/v2\/blog-subject?post=75961"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}