{"id":4235,"date":"2026-06-02T13:45:28","date_gmt":"2026-06-02T10:45:28","guid":{"rendered":"https:\/\/demo.erayonetim.com\/?post_type=faq&#038;p=4235"},"modified":"2026-06-02T13:46:51","modified_gmt":"2026-06-02T10:46:51","slug":"medical-device-market-access-technical-file-preparation","status":"publish","type":"faq","link":"https:\/\/demo.erayonetim.com\/en\/sss\/tibbi-cihaz-pazara-arz-teknik-dosya-hazirligi\/","title":{"rendered":"Why is the technical file important in the process of bringing medical devices to market?"},"content":{"rendered":"<div class=\"wpb-content-wrapper\"><div class=\"vc_row wpb_row row top-row wpb_custom_034b39d9bc6c6b310d69e39f0ccf274f\"><div class=\"vc_column_container col-md-12\"><div class=\"wpb_wrapper vc_column-inner\">\r\n\t<div class=\"wpb_text_column wpb_content_element wpb_custom_7c91d232724f73626cc933bd95b25ff0\" >\r\n\t\t<div class=\"wpb_wrapper\">\r\n\t\t\t<p>The technical file is the most fundamental document proving the safety and performance of your device. This file, which will be reviewed by approved organizations and the ministry, must be complete and directly determine your product&#039;s market approval.<\/p>\n\r\n\t\t<\/div>\r\n\t<\/div>\r\n<\/div><\/div><\/div>\n<\/div>","protected":false},"template":"","faq_cat":[],"class_list":["post-4235","faq","type-faq","status-publish","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/demo.erayonetim.com\/en\/wp-json\/wp\/v2\/faq\/4235","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/demo.erayonetim.com\/en\/wp-json\/wp\/v2\/faq"}],"about":[{"href":"https:\/\/demo.erayonetim.com\/en\/wp-json\/wp\/v2\/types\/faq"}],"wp:attachment":[{"href":"https:\/\/demo.erayonetim.com\/en\/wp-json\/wp\/v2\/media?parent=4235"}],"wp:term":[{"taxonomy":"faq_cat","embeddable":true,"href":"https:\/\/demo.erayonetim.com\/en\/wp-json\/wp\/v2\/faq_cat?post=4235"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}