{"id":8422,"date":"2013-04-24T10:02:44","date_gmt":"2013-04-24T09:02:44","guid":{"rendered":"http:\/\/catai.net\/blog\/?p=8422"},"modified":"2013-04-24T10:02:44","modified_gmt":"2013-04-24T09:02:44","slug":"finalmente-regulamos-el-software-medico","status":"publish","type":"post","link":"https:\/\/catai.net\/blog\/2013\/04\/finalmente-regulamos-el-software-medico\/","title":{"rendered":"Finalmente regulamos el software m\u00e9dico!!!"},"content":{"rendered":"<p>Un recurso propuesto por los reguladores internacionales en dispositivos m\u00e9dicos para centrarse en el tema de la regulaci\u00f3n del software m\u00e9dico, incluida las apps, pone de manifiesto en inter\u00e9s de muchas partes en avanzar en un marco com\u00fan para que esta regulaci\u00f3n se lleve a cabo. El\u00a0<strong><a href=\"http:\/\/www.imdrf.org\/\" target=\"_blank\">International Medical Device Regulators Forum (IMDRF)<\/a>,<\/strong>\u00a0un foro concebido en 2011 en el que forman parte muchos reguladores internacionales con la intenci\u00f3n de harmonizar el trabajo de estandarizaci\u00f3n internacional en el campo de los dispositivos m\u00e9dicos,\u00a0ha decido poner sobre la mesa la\u00a0estandarizaci\u00f3n del software m\u00e9dico, incluyendo apps m\u00e9dicas,\u00a0\u00a0software cl\u00ednico de apoyo y\u00a0decisi\u00f3n, historia cl\u00ednica electr\u00f3nica y cualquier otro software utilizado en healthcare que no sea un controlador (driver)\u00a0de un dispositivo m\u00e9dico.<\/p>\n<p>Por nuestro lado, llevamos ya tiempo anunciando la necesidad de la regulaci\u00f3n del software m\u00e9dico, como los apps compatibles con los SO m\u00f3viles como Android, iOS, etc. En el art\u00edculo <strong><a href=\"http:\/\/www.intechopen.com\/books\/advances-in-telemedicine-technologies-enabling-factors-and-scenarios\/quality-control-in-telemedicine-ce-label\" target=\"_blank\">Quality Control in Telemedicine &#8211; \u201cCE\u201d Label<\/a>\u00a0<\/strong>se comenta la importancia del marchamo o marca &#8220;CE Label&#8221; a la hora de regular los dispositivos y el software m\u00e9dico y en el art\u00edculo\u00a0<strong><a href=\"http:\/\/www.teide.net\/catai\/StandardsTelemedicine.pdf\" target=\"_blank\">Standards in Telemedicine<\/a>\u00a0<\/strong>se pone sobre la mesa la necesidad de una estandarizaci\u00f3n com\u00fan a nivel Europeo en cuanto a la conectividad y el control de calidad.<\/p>\n<p><a href=\"http:\/\/mobihealthnews.com\/21627\/international-regulators-focus-on-medical-software-including-apps\/\" target=\"_blank\">mobihealthnews.com | Enlace a noticia<\/a><\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Un recurso propuesto por los reguladores internacionales en dispositivos m\u00e9dicos para centrarse en el tema de la regulaci\u00f3n del software m\u00e9dico, incluida las apps, pone de manifiesto en inter\u00e9s de muchas partes en avanzar en un marco com\u00fan para que esta regulaci\u00f3n se lleve a cabo. El\u00a0International Medical Device Regulators Forum (IMDRF),\u00a0un foro concebido en [&hellip;]<\/p>\n","protected":false},"author":5,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"give_campaign_id":0,"_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_hide_featured_image":false,"_jetpack_featured_image_duplicate_dismissed":0,"_jetpack_feature_clip_id":0,"_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":false,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2},"jetpack_post_was_ever_published":false},"categories":[11,1,35,3,40,7,13,24,26,28,29],"tags":[],"class_list":["post-8422","post","type-post","status-publish","format-standard","hentry","category-diagnostico-no-invasivo","category-general","category-idi","category-informes","category-innovacion","category-oferrer-roca","category-phealth","category-productividad","category-publicaciones","category-sanidad","category-seguridad"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Finalmente regulamos el software m\u00e9dico!!! | Telemedicina<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/catai.net\/blog\/2013\/04\/finalmente-regulamos-el-software-medico\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Finalmente regulamos el software m\u00e9dico!!! | Telemedicina\" \/>\n<meta property=\"og:description\" content=\"Un recurso propuesto por los reguladores internacionales en dispositivos m\u00e9dicos para centrarse en el tema de la regulaci\u00f3n del software m\u00e9dico, incluida las apps, pone de manifiesto en inter\u00e9s de muchas partes en avanzar en un marco com\u00fan para que esta regulaci\u00f3n se lleve a cabo. 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