{"id":20399,"date":"2024-10-03T23:30:10","date_gmt":"2024-10-03T21:30:10","guid":{"rendered":"https:\/\/www.m-q.ch\/de\/?p=20399"},"modified":"2024-10-01T10:31:33","modified_gmt":"2024-10-01T08:31:33","slug":"medical-devices-ordinance-position-swissmedic","status":"publish","type":"post","link":"https:\/\/www.m-q.ch\/en\/medical-devices-ordinance-position-swissmedic\/","title":{"rendered":"Medical Devices Ordinance: Swissmedic's position"},"content":{"rendered":"<div class=\"swpm-post-not-logged-in-msg\">You need to be logged in to view this content. Please <a class=\"swpm-login-link\" href=\"https:\/\/www.m-q.ch\/en\/login\/\">Log In<\/a>. Not a Member? <a href=\"https:\/\/www.m-q.ch\/en\/register\/\">Join Us<\/a><\/div>","protected":false},"excerpt":{"rendered":"<p>In issue 7-8\/2024, an article dealt with the consequences of the EU Medical Devices Regulation for the Swiss medtech industry. The report focused on the risk that an \"approval backlog\" could jeopardize the security of supply of medical devices in hospitals. Andr\u00e9 Breisinger from Swissmedic, the Swiss regulatory and supervisory authority for medicinal products and medical devices, provides additional information.<\/p>","protected":false},"author":364,"featured_media":20398,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[4443,3303],"tags":[4906,5595,3490,5011],"class_list":["post-20399","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-abo","category-qualitaetsmanagement","tag-medizinprodukteverordnung","tag-patientensicherheit","tag-schweiz","tag-swissmedic"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.2 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Medizinprodukteverordnung: Standpunkt Swissmedic - MQ Management und Qualit\u00e4t<\/title>\n<meta name=\"description\" content=\"In der Ausgabe 7-8\/2024 befasste sich ein Artikel mit den Folgen der EU-Medizinprodukteverordnung f\u00fcr die Schweizer Medtech-Branche.\" \/>\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.m-q.ch\/en\/medical-devices-ordinance-position-swissmedic\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Medizinprodukteverordnung: Standpunkt Swissmedic - 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