{"id":4236,"date":"2026-06-02T13:48:51","date_gmt":"2026-06-02T10:48:51","guid":{"rendered":"https:\/\/demo.erayonetim.com\/?post_type=faq&#038;p=4236"},"modified":"2026-06-02T13:49:02","modified_gmt":"2026-06-02T10:49:02","slug":"tracking-national-international-medical-device-regulatory-changes","status":"publish","type":"faq","link":"https:\/\/demo.erayonetim.com\/en\/sss\/ulusal-uluslararasi-tibbi-cihaz-mevzuat-degisiklikleri-takibi\/","title":{"rendered":"How to Keep Track of Updated National and International Medical Device Regulation Changes?"},"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>Medical device regulations are constantly being updated. As ERA Management, we closely monitor these global and national regulatory changes on behalf of your company, keeping your system up-to-date without interruption.<\/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-4236","faq","type-faq","status-publish","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/demo.erayonetim.com\/en\/wp-json\/wp\/v2\/faq\/4236","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=4236"}],"wp:term":[{"taxonomy":"faq_cat","embeddable":true,"href":"https:\/\/demo.erayonetim.com\/en\/wp-json\/wp\/v2\/faq_cat?post=4236"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}