{"id":9547,"date":"2026-05-08T14:06:32","date_gmt":"2026-05-08T12:06:32","guid":{"rendered":"https:\/\/ekfz.uni-goettingen.de\/mitteilungen\/april-22-2026-i-ekfz-academy-workshop\/"},"modified":"2026-05-08T14:08:45","modified_gmt":"2026-05-08T12:08:45","slug":"april-22-2026-i-ekfz-academy-workshop","status":"publish","type":"cdp_press_release","link":"https:\/\/ekfz.uni-goettingen.de\/en\/mitteilungen\/april-22-2026-i-ekfz-academy-workshop\/","title":{"rendered":"How can medical device approval be achieved in a complex regulatory environment?"},"content":{"rendered":"<p>This central question was addressed as part of the EKFZ Academy workshop &#8220;Medical Devices \u2013 Quality and Regulatory Overview&#8221;, led by Dr. Sabine Hauck.<\/p>\n","protected":false},"featured_media":0,"template":"","cdp_year":[234],"class_list":["post-9547","cdp_press_release","type-cdp_press_release","status-publish","hentry","cdp_year-2026-en"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.9 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>How can medical device approval be achieved in a complex regulatory environment? 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