{"id":226227,"date":"2023-04-12T10:15:42","date_gmt":"2023-04-12T08:15:42","guid":{"rendered":"https:\/\/www.tuleap.org\/?page_id=226227"},"modified":"2026-01-30T11:54:41","modified_gmt":"2026-01-30T10:54:41","slug":"replay-webinaire-iso13485-iec62304-maitrisez-vos-processus","status":"publish","type":"replay","link":"https:\/\/www.tuleap.com\/fr\/replay\/replay-webinaire-iso13485-iec62304-maitrisez-vos-processus\/","title":{"rendered":"ISO 13485 &#8211; IEC 62304 : ma\u00eetrisez vos processus pour simplifier les audits"},"content":{"rendered":"<h2>Programme<\/h2>\n<ul>\n<li>Structurer vos exigences, tests, anomalies et risques pour garantir la tra\u00e7abilit\u00e9<\/li>\n<li>R\u00e9pondre aux exigences de la norme IEC 62304 et ISO 13485 avec un outil unique<\/li>\n<li>Aligner vos \u00e9quipes R&amp;D, qualit\u00e9 et r\u00e9glementaire sans cr\u00e9er de silos<\/li>\n<li>Pr\u00e9parer vos audits sans stress (et sans tableurs)<\/li>\n<li>Exemple concret d\u2019un processus qualit\u00e9 outill\u00e9 avec Tuleap<\/li>\n<li>Retours d\u2019exp\u00e9rience : T\u00e9moignages de professionnels de la medtech<\/li>\n<\/ul>\n","protected":false},"author":24,"featured_media":259812,"template":"","format":[207],"meta":{"_acf_changed":false,"content-type":"","inline_featured_image":false,"footnotes":""},"affichage":[],"enjeu":[131,54],"fonctions":[60,62],"format-ressource":[198],"industries":[78],"class_list":["post-226227","replay","type-replay","status-publish","format-standard","has-post-thumbnail","hentry","enjeu-gestion-de-projet","enjeu-qualite","fonctions-gestion-de-projet","fonctions-gestion-des-risques-et-de-la-qualite","format-webinaire","format-ressource-webinaire","industries-sante-et-medical"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.7 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>ISO 13485 - IEC 62304 : ma\u00eetrisez vos processus pour simplifier les audits - Tuleap<\/title>\n<meta name=\"description\" content=\"Dans la Medtech, \u00eates-vous pr\u00eat \u00e0 prouver aux auditeurs que vos logiciels de DM sont conformes ? 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