{"id":59405,"date":"2022-01-05T16:04:26","date_gmt":"2022-01-05T15:04:26","guid":{"rendered":"https:\/\/www.iccas.de\/?p=59405"},"modified":"2022-02-02T16:09:05","modified_gmt":"2022-02-02T15:09:05","slug":"iccas-re-zertifiziert","status":"publish","type":"post","link":"https:\/\/www.iccas.de\/en\/iccas-re-zertifiziert\/?&lang=en","title":{"rendered":"ICCAS recertified"},"content":{"rendered":"<p><span data-contrast=\"auto\">C<\/span><span data-contrast=\"auto\">ompanies can<\/span><span data-contrast=\"auto\"> continue<\/span><span data-contrast=\"auto\"> to implement cooperation projects with ICCAS according to the German Medical Products Law DIN EN ISO 13485. <\/span><!--more--><span data-contrast=\"auto\">This is ensured by the successful ISO <\/span><span data-contrast=\"auto\">re<\/span><span data-contrast=\"auto\">certification, which <\/span><span data-contrast=\"auto\">was renewed <\/span><span data-contrast=\"auto\">for <\/span><span data-contrast=\"auto\">ICCAS\u2019 <\/span><span data-contrast=\"auto\">research and development of medical device software.<\/span><span data-ccp-props=\"{\"134233117\":true,\"134233118\":true,\"201341983\":0,\"335551550\":6,\"335551620\":6,\"335559740\":240}\">\u00a0<\/span><span data-contrast=\"auto\">For companies<\/span><span data-contrast=\"auto\">,<\/span><span data-contrast=\"auto\"> this means <\/span><span data-contrast=\"auto\">that the software systems<\/span><span data-contrast=\"auto\"> developed in cooperation with ICCAS <\/span><span data-contrast=\"auto\">fulfil the<\/span><span data-contrast=\"auto\"> requirements of quality standards of the medical products law<\/span><span data-contrast=\"auto\"> and can be implemented by purpose<\/span><span data-contrast=\"auto\">. <\/span><span data-contrast=\"auto\">P<\/span><span data-contrast=\"auto\">roduction processes and methods take place under defined guidelines<\/span><span data-contrast=\"auto\">,<\/span><span data-contrast=\"auto\"> which ensure a high quality of the products.\u00a0<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Companies can continue to implement cooperation projects with ICCAS according to the German Medical Products Law DIN EN ISO 13485.<\/p>\n","protected":false},"author":31,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[1],"tags":[],"class_list":["post-59405","post","type-post","status-publish","format-standard","hentry","category-news"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.8 - 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