{"id":248846,"date":"2025-11-23T22:31:52","date_gmt":"2025-11-23T21:31:52","guid":{"rendered":"https:\/\/www.tuleap.com\/?post_type=webinaires&p=248846"},"modified":"2026-01-27T15:50:45","modified_gmt":"2026-01-27T14:50:45","slug":"tracabilite-des-dispositifs-et-logiciels-medicaux","status":"publish","type":"webinaires","link":"https:\/\/www.tuleap.com\/fr\/webinaires\/tracabilite-des-dispositifs-et-logiciels-medicaux\/","title":{"rendered":"Tra\u00e7abilit\u00e9 des dispositifs et logiciels m\u00e9dicaux : Comment garantir conformit\u00e9 et efficacit\u00e9 sans complexit\u00e9 ?"},"content":{"rendered":"

Garantir la conformit\u00e9 aux normes comme IEC 62304 ou ISO 13485 n\u2019est pas une option. D\u00e9couvrez comment structurer vos projets de d\u00e9veloppement pour assurer une tra\u00e7abilit\u00e9 compl\u00e8te, sans freiner l\u2019innovation.<\/p>\n

Vous cherchez \u00e0 simplifier la gestion de la conformit\u00e9 de vos dispositifs m\u00e9dicaux et logiciels?
\nNous vous montrerons comment la centralisation des exigences, l\u2019automatisation des processus r\u00e9glementaires et leur int\u00e9gration fluide dans le cycle de d\u00e9veloppement permettent de r\u00e9pondre aux exigences normatives, sans alourdir vos \u00e9quipes avec une charge administrative excessive.<\/p>\n

Ce que vous allez apprendre :<\/p>\n

– Structurer vos exigences, tests, anomalies et risques pour garantir la tra\u00e7abilit\u00e9
\n– R\u00e9pondre aux exigences de la norme IEC 62304\u00a0et ISO 13485 avec un outil unique
\n– Aligner vos \u00e9quipes R&D, qualit\u00e9 et r\u00e9glementaire sans cr\u00e9er de silos
\n– Pr\u00e9parer vos audits sans stress (et sans tableurs)
\n– Exemple concret d\u2019un processus qualit\u00e9 outill\u00e9 avec Tuleap
\n– Retours d\u2019exp\u00e9rience : T\u00e9moignages de professionnels de la medtech<\/p>\n

\ud83e\uddd1\u200d\u2695\ufe0f Pour qui est ce webinaire ?<\/p>\n

Ce webinaire s\u2019adresse \u00e0 vous si vous \u00eates :
\n– Responsable qualit\u00e9 ou conformit\u00e9 dans la MedTech
\n–\u00a0Chef de projet logiciel ou syst\u00e8me
\n– Ing\u00e9nieur R&D, validation ou affaires r\u00e9glementaires
\n– Fournisseur de logiciels embarqu\u00e9s ou SaMD<\/p>\n","protected":false},"author":24,"featured_media":259811,"template":"","meta":{"_acf_changed":false,"content-type":"","inline_featured_image":false,"footnotes":""},"affichage":[],"enjeu":[54],"fonctions":[60,65,64],"industries":[78],"type-de-webinaire":[85],"class_list":["post-248846","webinaires","type-webinaires","status-publish","has-post-thumbnail","hentry","enjeu-qualite","fonctions-gestion-de-projet","fonctions-product-management","fonctions-transformation-agile","industries-sante-et-medical","type-de-webinaire-passes"],"acf":[],"yoast_head":"\nTra\u00e7abilit\u00e9 des dispositifs et logiciels m\u00e9dicaux : Comment garantir conformit\u00e9 et efficacit\u00e9 sans complexit\u00e9 ? - Tuleap<\/title>\n<meta name=\"robots\" content=\"noindex, follow\" \/>\n<meta property=\"og:locale\" content=\"fr_FR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Tra\u00e7abilit\u00e9 des dispositifs et logiciels m\u00e9dicaux : Comment garantir conformit\u00e9 et efficacit\u00e9 sans complexit\u00e9 ? - Tuleap\" \/>\n<meta property=\"og:description\" content=\"Garantir la conformit\u00e9 aux normes comme IEC 62304 ou ISO 13485 n\u2019est pas une option. 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