{"id":20825,"date":"2024-12-17T00:33:25","date_gmt":"2024-12-16T23:33:25","guid":{"rendered":"https:\/\/www.m-q.ch\/de\/?p=20825"},"modified":"2024-12-11T14:13:38","modified_gmt":"2024-12-11T13:13:38","slug":"pour-une-meilleure-compliance-dans-la-technique-medicale","status":"publish","type":"post","link":"https:\/\/www.m-q.ch\/fr\/pour-une-meilleure-compliance-dans-la-technique-medicale\/","title":{"rendered":"Pour une meilleure compliance dans la technologie m\u00e9dicale"},"content":{"rendered":"<div class=\"swpm-post-not-logged-in-msg\">Vous devez \u00eatre connect\u00e9 pour voir ce contenu. Veuillez <a class=\"swpm-login-link\" href=\"https:\/\/www.m-q.ch\/fr\/login\/\">Se connecter<\/a>. Pas un membre ? <a href=\"https:\/\/www.m-q.ch\/fr\/sinscrire\/\">Nous Rejoindre<\/a><\/div>","protected":false},"excerpt":{"rendered":"<p>Des r\u00e8gles strictes r\u00e9gissent la gestion de la qualit\u00e9 dans le domaine de la technologie m\u00e9dicale. Des normes exhaustives, telles que la norme DIN EN ISO 13485 ou la Medical Device Regulation (MDR) de l'UE, exigent une documentation sans faille des processus de qualit\u00e9 qui, en cas d'urgence, sont d\u00e9terminants pour la s\u00e9curit\u00e9 et la sant\u00e9 des patients.<\/p>","protected":false},"author":364,"featured_media":20823,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[4443,3303],"tags":[5751,3781,5752,5216,3327],"class_list":["post-20825","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-abo","category-qualitaetsmanagement","tag-arbeitserleichterung","tag-automation","tag-dokumentation","tag-medizintechnik","tag-qualitaetsmanagement"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.2 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>F\u00fcr bessere Compliance in der Medizintechnik - 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