{"id":3883,"date":"2022-10-11T17:17:56","date_gmt":"2022-10-11T09:17:56","guid":{"rendered":"https:\/\/regask.com\/?p=3883"},"modified":"2024-11-22T05:27:00","modified_gmt":"2024-11-21T21:27:00","slug":"ensayos-clinicos-descentralizados-cruzados","status":"publish","type":"post","link":"https:\/\/regask.com\/es\/decentralized-clinical-trials-cros\/","title":{"rendered":"Ensayos cl\u00ednicos descentralizados: c\u00f3mo las CRO pueden beneficiarse\u2026"},"content":{"rendered":"<p>A medida que la pandemia de COVID-19 contin\u00faa interrumpiendo la investigaci\u00f3n cl\u00ednica, existe una mayor necesidad por parte de la industria farmac\u00e9utica y de CRO de implementar ensayos cl\u00ednicos descentralizados o h\u00edbridos (DCT) para mejorar la eficiencia de los ensayos cl\u00ednicos.<\/p>\n<p><strong>Lea nuestro estudio de caso para saber c\u00f3mo RegASK ayuda a las CRO a cumplir con los requisitos reglamentarios para implementar DCT en diferentes pa\u00edses.<\/strong><\/p>\n<h2 class=\"h4\"><strong>Desaf\u00edo<\/strong><\/h2>\n<p>Una organizaci\u00f3n de investigaci\u00f3n virtual buscaba obtener informaci\u00f3n regulatoria sobre las DCT en 16 pa\u00edses\/regiones para orientar mejor la ejecuci\u00f3n de sus ensayos cl\u00ednicos. Sin embargo, navegar por el panorama regulatorio de las DCT y cumplir con la normativa no es f\u00e1cil. Las regulaciones var\u00edan considerablemente de un pa\u00eds a otro y no siempre est\u00e1n completamente desarrolladas. Las organizaciones de ciencias de la vida y CRO est\u00e1n sujetas a cambios regulatorios, lo que genera incertidumbre y retrasos en la implementaci\u00f3n de ensayos cl\u00ednicos.<\/p>\n<h2 class=\"h4\"><strong>Soluci\u00f3n<\/strong><\/h2>\n<p>RegASK brind\u00f3 soluciones integrales de asuntos regulatorios sobre DCT, que incluyen:<\/p>\n<ul>\n<li>Lleno <strong>Gu\u00edas tur\u00edsticas<\/strong> Responder preguntas relacionadas con las regulaciones de ensayos cl\u00ednicos, desde el dise\u00f1o del estudio hasta una gu\u00eda paso a paso sobre c\u00f3mo registrar un ensayo cl\u00ednico.<\/li>\n<li>A <strong>Tarjeta de conocimiento<\/strong> Responder preguntas regulatorias espec\u00edficas<\/li>\n<li>Una hoja de ruta del proceso de presentaci\u00f3n<\/li>\n<li>Acceso a la <a href=\"https:\/\/regask.com\/es\/our-solution\/#detect\" target=\"_blank\" rel=\"noopener\">Plataforma de monitoreo regulatorio RegAlert<\/a> que utiliza IA para proporcionar actualizaciones a la <strong>Gu\u00edas tur\u00edsticas<\/strong> y <strong>Tarjeta de conocimiento<\/strong><\/li>\n<\/ul>\n<h2 class=\"h4\"><strong>Resultados<\/strong><\/h2>\n<p>El cliente adquiri\u00f3 experiencia regulatoria espec\u00edfica que no exist\u00eda internamente y redujo el costo de monitoreo (sin necesidad de contratar personal adicional). M\u00e1s importante a\u00fan, obtuvo tranquilidad respecto a los cambios regulatorios en las DCT, lo que le permiti\u00f3 concentrarse en expandir su negocio.<\/p>","protected":false},"excerpt":{"rendered":"<p>A medida que la pandemia de COVID-19 contin\u00faa interrumpiendo la investigaci\u00f3n cl\u00ednica, la industria farmac\u00e9utica y las CRO tienen una mayor necesidad de implementar ensayos cl\u00ednicos descentralizados o h\u00edbridos (ECD) para mejorar la eficiencia de los ensayos cl\u00ednicos. Lea nuestro caso pr\u00e1ctico para saber c\u00f3mo RegASK ayuda a las CRO a cumplir con los requisitos regulatorios para la implementaci\u00f3n de ECD en diferentes pa\u00edses. Desaf\u00edo\u2026<\/p>","protected":false},"author":39,"featured_media":3954,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[17,21],"tags":[],"class_list":["post-3883","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-case-study","category-pharma-and-biotech"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v28.4 (Yoast SEO v28.4) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>Decentralized CT: CROs Benefit from RegGuides | RegASK<\/title>\n<meta name=\"description\" content=\"Learn how RegASK assists CROs in fulfilling the regulatory requirements for implementing Decentralized Clinical Trials across countries.\u00a0\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/regask.com\/es\/ensayos-clinicos-descentralizados-cruzados\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Decentralized Clinical Trials: How CROs can benefit from our RegGuides\" \/>\n<meta property=\"og:description\" content=\"Learn how RegASK assists CROs in fulfilling the regulatory requirements for implementing Decentralized Clinical Trials across countries.\u00a0\" \/>\n<meta property=\"og:url\" content=\"https:\/\/regask.com\/es\/ensayos-clinicos-descentralizados-cruzados\/\" \/>\n<meta property=\"og:site_name\" content=\"RegASK\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/RegASKRegulatoryAffairs\/\" \/>\n<meta property=\"article:published_time\" content=\"2022-10-11T09:17:56+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2024-11-21T21:27:00+00:00\" \/>\n<meta property=\"og:image\" 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