{"id":19734,"date":"2021-12-14T12:19:30","date_gmt":"2021-12-14T11:19:30","guid":{"rendered":"https:\/\/www.thema-med.com\/?p=19734"},"modified":"2021-12-14T12:19:30","modified_gmt":"2021-12-14T11:19:30","slug":"swiss-exit-que-requisitos-deben-cumplir-ahora-los-fabricantes-de-productos-medicos-de-la-ue","status":"publish","type":"post","link":"https:\/\/www.thema-med.com\/es\/2021\/12\/14\/swiss-exit-que-requisitos-deben-cumplir-ahora-los-fabricantes-de-productos-medicos-de-la-ue\/","title":{"rendered":"Swiss Exit: \u00bfQu\u00e9 requisitos deben cumplir ahora los Fabricantes de Dispositivos M\u00e9dicos de la UE?"},"content":{"rendered":"\n

Desde el 26 de mayo 2021, Suiza se ha convertido de pleno derecho en un tercer pa\u00eds y los Fabricantes suizos reciben el mismo trato que cualquier otro fabricante fuera de la UE. Por lo tanto, los Fabricantes no suizos deber\u00e1n designar Representantes Autorizados Suizos y Importadores con sede en Suiza. En otras palabras, los Fabricantes de Dispositivos M\u00e9dicos <\/strong>con sede fuera del territorio suizo deben nombrar el \u201cSwiss Representative<\/strong>\u201d (tambi\u00e9n conocido como Swiss REP o CH REP<\/strong>) con sede en Suiza, cuyo nombre debe mencionarse en el producto y en el etiquetado, as\u00ed como los posibles importadores para Suiza.<\/p>\n\n\n\n

Descubre los servicios de asesoramiento estrat\u00e9gico-regulador Thema<\/a><\/strong><\/p>\n","protected":false},"excerpt":{"rendered":"

Desde el 26 de mayo 2021, Suiza se ha convertido de pleno derecho en un tercer pa\u00eds y los Fabricantes suizos […]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"categories":[891,1443],"tags":[],"class_list":["post-19734","post","type-post","status-publish","format-standard","hentry","category-faq-es","category-suiza-faq-es"],"acf":[],"yoast_head":"\n\u00bfQu\u00e9 requisitos deben cumplir los Fabricantes UE de productos m\u00e9dicos?<\/title>\n<meta name=\"description\" content=\"Los Fabricantes de Dispositivos M\u00e9dicos con sede fuera del territorio suizo deben nombrar el \u201cSwiss Representative\u201d (Swiss REP o CH REP) con sede en Suiza\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.thema-med.com\/es\/2021\/12\/14\/swiss-exit-que-requisitos-deben-cumplir-ahora-los-fabricantes-de-productos-medicos-de-la-ue\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"\u00bfQu\u00e9 requisitos deben cumplir los Fabricantes UE de productos m\u00e9dicos?\" \/>\n<meta property=\"og:description\" content=\"Los Fabricantes de Dispositivos M\u00e9dicos con sede fuera del territorio suizo deben nombrar el \u201cSwiss Representative\u201d (Swiss REP o CH REP) con sede en Suiza\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.thema-med.com\/es\/2021\/12\/14\/swiss-exit-que-requisitos-deben-cumplir-ahora-los-fabricantes-de-productos-medicos-de-la-ue\/\" \/>\n<meta property=\"og:site_name\" content=\"Thema - 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