{"id":1659,"date":"2022-08-09T15:46:21","date_gmt":"2022-08-09T13:46:21","guid":{"rendered":"https:\/\/www.tertia-med.de\/?p=1659"},"modified":"2022-08-09T15:46:21","modified_gmt":"2022-08-09T13:46:21","slug":"bruesseler-zulassungsregeln-vor-dem-update","status":"publish","type":"post","link":"https:\/\/www.tertia-med.de\/en\/bruesseler-zulassungsregeln-vor-dem-update\/","title":{"rendered":"Br\u00fcsseler Zulassungsregeln vor dem Update"},"content":{"rendered":"<p>Die Frage, ob aufgrund einer EU-Medizinprodukterichtlinie (MDR) Medizinprodukte knapp werden, wird hei\u00df diskutiert. F\u00fcr den GKV-Spitzenverband sind solche Bef\u00fcrchtungen gro\u00dfteils Nebelkerzen. Die Medtech-Industrie verschafft sich derweil in Br\u00fcssel Geh\u00f6r. \u201eDie EU-Medizinprodukteverordnung ist ein wichtiger Fortschritt, denn sie dient in erster Linie dem Schutz der Patientinnen und Patienten &#8230;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Die Frage, ob aufgrund einer EU-Medizinprodukterichtlinie (MDR) Medizinprodukte knapp werden, wird hei\u00df diskutiert. F\u00fcr den GKV-Spitzenverband sind solche Bef\u00fcrchtungen gro\u00dfteils Nebelkerzen. Die Medtech-Industrie verschafft sich derweil in Br\u00fcssel Geh\u00f6r. \u201eDie EU-Medizinprodukteverordnung ist ein wichtiger Fortschritt, denn sie dient in erster Linie dem Schutz der Patientinnen und Patienten &#8230;<\/p>\n","protected":false},"author":1,"featured_media":1660,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[16],"tags":[],"class_list":["post-1659","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-uncategorized"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Br\u00fcsseler Zulassungsregeln vor dem Update - Tertia Med<\/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:\/\/www.tertia-med.de\/en\/bruesseler-zulassungsregeln-vor-dem-update\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Br\u00fcsseler Zulassungsregeln vor dem Update - Tertia Med\" \/>\n<meta property=\"og:description\" content=\"Die Frage, ob aufgrund einer EU-Medizinprodukterichtlinie (MDR) Medizinprodukte knapp werden, wird hei\u00df diskutiert. 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