{"id":17797,"date":"2026-02-06T12:54:53","date_gmt":"2026-02-06T09:54:53","guid":{"rendered":"https:\/\/www.d-tek.com.tr\/?p=17797"},"modified":"2026-02-13T19:41:09","modified_gmt":"2026-02-13T16:41:09","slug":"2025-tibbi-laboratuvar-yonetmeligi-sahadan-degerlendirme","status":"publish","type":"post","link":"https:\/\/www.d-tek.com.tr\/en\/2025-tibbi-laboratuvar-yonetmeligi-sahadan-degerlendirme\/","title":{"rendered":"A Field and International Standards Perspective on the 2025 Medical Laboratory Regulation"},"content":{"rendered":"<div id=\"ez-toc-container\" class=\"ez-toc-v2_0_82_2 counter-flat ez-toc-counter ez-toc-grey ez-toc-container-direction\">\n<div class=\"ez-toc-title-container\">\n<p class=\"ez-toc-title\" style=\"cursor:inherit\">Highlighted Topics<\/p>\n<span class=\"ez-toc-title-toggle\"><a href=\"#\" class=\"ez-toc-pull-right ez-toc-btn ez-toc-btn-xs ez-toc-btn-default ez-toc-toggle\" aria-label=\"Toggle Table of Content\"><span class=\"ez-toc-js-icon-con\"><span class=\"\"><span class=\"eztoc-hide\" style=\"display:none;\">Toggle<\/span><span class=\"ez-toc-icon-toggle-span\"><svg style=\"fill: #999;color:#999\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" class=\"list-377408\" width=\"20px\" height=\"20px\" viewbox=\"0 0 24 24\" fill=\"none\"><path d=\"M6 6H4v2h2V6zm14 0H8v2h12V6zM4 11h2v2H4v-2zm16 0H8v2h12v-2zM4 16h2v2H4v-2zm16 0H8v2h12v-2z\" fill=\"currentColor\"><\/path><\/svg><svg style=\"fill: #999;color:#999\" class=\"arrow-unsorted-368013\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" width=\"10px\" height=\"10px\" viewbox=\"0 0 24 24\" version=\"1.2\" baseprofile=\"tiny\"><path d=\"M18.2 9.3l-6.2-6.3-6.2 6.3c-.2.2-.3.4-.3.7s.1.5.3.7c.2.2.4.3.7.3h11c.3 0 .5-.1.7-.3.2-.2.3-.5.3-.7s-.1-.5-.3-.7zM5.8 14.7l6.2 6.3 6.2-6.3c.2-.2.3-.5.3-.7s-.1-.5-.3-.7c-.2-.2-.4-.3-.7-.3h-11c-.3 0-.5.1-.7.3-.2.2-.3.5-.3.7s.1.5.3.7z\"\/><\/svg><\/span><\/span><\/span><\/a><\/span><\/div>\n<nav><ul class='ez-toc-list ez-toc-list-level-1 ez-toc-columns-2' ><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-1\" href=\"https:\/\/www.d-tek.com.tr\/en\/2025-tibbi-laboratuvar-yonetmeligi-sahadan-degerlendirme\/#2025_Tibbi_Laboratuvar_Yonetmeligi_Neleri_Degistiriyor\" >What Changes Does the 2025 Medical Laboratory Regulation Bring?<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-2\" href=\"https:\/\/www.d-tek.com.tr\/en\/2025-tibbi-laboratuvar-yonetmeligi-sahadan-degerlendirme\/#Belirlilik_Uygulanabilirlik_ve_Dijitallesme_Acisindan_Degerlendirme\" >Assessment in Terms of Specificity, Applicability, and Digitalization<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-3\" href=\"https:\/\/www.d-tek.com.tr\/en\/2025-tibbi-laboratuvar-yonetmeligi-sahadan-degerlendirme\/#Tanimlar_Kavram_Netligi_Olmadan_Uygulama_ve_Hasta_Guvenligi_Risk_Altina_Girebilir\" >Definitions: Without conceptual clarity, practice and patient safety can be jeopardized.<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-4\" href=\"https:\/\/www.d-tek.com.tr\/en\/2025-tibbi-laboratuvar-yonetmeligi-sahadan-degerlendirme\/#ISO_15189_Perspektifinden_Bakildiginda\" >Viewed from the perspective of ISO 15189<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-5\" href=\"https:\/\/www.d-tek.com.tr\/en\/2025-tibbi-laboratuvar-yonetmeligi-sahadan-degerlendirme\/#Fiziksel_Kriterler_Metrekare_mi_Risk_Temelli_mi\" >Physical Criteria: Square Meter or Risk-Based?<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-6\" href=\"https:\/\/www.d-tek.com.tr\/en\/2025-tibbi-laboratuvar-yonetmeligi-sahadan-degerlendirme\/#Personel_ve_Yetkinlik_En_Kritik_Eksik_Alanlardan_Biri\" >Personnel and Competence: One of the Most Critical Deficiency Areas<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-7\" href=\"https:\/\/www.d-tek.com.tr\/en\/2025-tibbi-laboratuvar-yonetmeligi-sahadan-degerlendirme\/#Bilgi_Sistemleri_ve_Dijitallesme_Firsat_mi_Risk_mi\" >Information Systems and Digitalization: Opportunity or Risk?<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-8\" href=\"https:\/\/www.d-tek.com.tr\/en\/2025-tibbi-laboratuvar-yonetmeligi-sahadan-degerlendirme\/#Sahadan_Gelen_Ses_Anket_Bulgulari_Ne_Diyor\" >Voice from the Field: What Do the Survey Findings Say?<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-9\" href=\"https:\/\/www.d-tek.com.tr\/en\/2025-tibbi-laboratuvar-yonetmeligi-sahadan-degerlendirme\/#Sonuc_Iyi_Niyet_Iyilestirilmesi_Gereken_Yapisallik\" >Conclusion: Good Intentions, Structural Issues Needing Improvement<\/a><\/li><\/ul><\/nav><\/div>\n<h2><span class=\"ez-toc-section\" id=\"2025_Tibbi_Laboratuvar_Yonetmeligi_Neleri_Degistiriyor\"><\/span>What Changes Does the 2025 Medical Laboratory Regulation Bring?<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p><span style=\"font-size: 16px;\">While medical laboratories in T\u00fcrkiye were preparing for the 2024 Medical Laboratory Regulation by June 2026, a new regulation with a changed scope was published on October 24, 2025. It entered into force on the day of its publication. Besides medical (clinical) laboratories, genetic laboratories, R&amp;D laboratories, external quality assessment program providers, and medical laboratories providing training were also included within the scope of this regulation. This situation has sparked considerable debate, particularly among competent individuals who understand the separation and interaction of research, service, and education fields.<\/span><\/p>\n<p><span style=\"font-size: 16px;\"><em>As someone who has been involved at national and international levels in the creation, development, and publication processes of the TS EN ISO 15189 \u201cMedical Laboratories \u2013 Requirements for Quality and Competence\u201d Standard, I would like to share the following point:<\/em><\/span><\/p>\n<p><span style=\"font-size: 16px;\"><em>Initially, the term &quot;clinical laboratory&quot; was used. However, because this term did not adequately express the medical field, the term &quot;medical laboratory&quot; was adopted; and it was explicitly added to the definitions and explanations that the ISO 15189 Standard is specific to laboratories providing clinical services.<\/em><\/span><\/p>\n<p><span style=\"font-size: 16px;\">We wanted to present the 2025 Regulation, which is astonishing in terms of scientific rigor and applicability, for evaluation based on legal regulations, ISO 15189 standards, and information gathered from the field. The interview video can be accessed via the URL at the end of the article. Below is a summary of the discussions, highlighting the main points:<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"Belirlilik_Uygulanabilirlik_ve_Dijitallesme_Acisindan_Degerlendirme\"><\/span><span style=\"font-size: 16px;\"><strong>Assessment in Terms of Specificity, Applicability, and Digitalization<\/strong><\/span><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-size: 16px;\">Published on October 24, 2025 <strong>\u201c&quot;Regulation on Medical Laboratory Services and Advanced Technology Medical Laboratory Applications&quot; (2025 Medical Laboratory Regulation)<\/strong>, The regulation was presented as a significant milestone in the field of medical laboratories. It expanded the scope by repealing previous regulations, bringing genetic, advanced technology, and research and development activities, in addition to diagnostic laboratories, under the same framework.<\/span><\/p>\n<p><span style=\"font-size: 16px;\">However, when viewed from the field, from standards, and from international practices, this expansion... <strong>Certainty, risk-based approach, and feasibility.<\/strong> It appears that this also raises serious questions.<\/span><\/p>\n<p><span style=\"font-size: 16px;\">This article discusses the regulations. <strong>legal structure<\/strong>, <strong>ISO 15189 compliance<\/strong>, <strong>field applications<\/strong> And <strong>digital health perspective<\/strong> It is discussed from this perspective.<\/span><\/p>\n<p><span style=\"font-size: 16px;\">With the 2025 Medical Laboratory Regulation, the inspection approach will be &quot;\u201c<strong>How is it implemented in the field?<\/strong>\u201dIt seems to be shifting towards the &quot;...&quot; axis. This may be a correct orientation in principle. However, the fundamental problem here is: <strong>Regulations that do not clearly define how they should be implemented produce differing interpretations rather than uniformity of application in the field; this can create significant risks to patient safety.<\/strong><\/span><\/p>\n<p><span style=\"font-size: 16px;\">The regulation is quite comprehensive in terms of its articles, paragraphs, and clauses. However:<\/span><\/p>\n<ul>\n<li><span style=\"font-size: 16px;\">It is challenging to track which article and paragraph the clauses are based on.,<\/span><\/li>\n<li><span style=\"font-size: 16px;\">Multiple different topics are addressed together in a single article.,<\/span><\/li>\n<li><span style=\"font-size: 16px;\">Definitions are not always consistent with scientific and international terminology.<\/span><\/li>\n<\/ul>\n<p><span style=\"font-size: 16px;\">This situation places a significant burden on laboratories, especially during the preparation process.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"Tanimlar_Kavram_Netligi_Olmadan_Uygulama_ve_Hasta_Guvenligi_Risk_Altina_Girebilir\"><\/span><span style=\"font-size: 16px;\"><strong>Definitions: Without conceptual clarity, practice and patient safety can be jeopardized.<\/strong><\/span><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-size: 16px;\">One of the most critical elements for the effective and safe implementation of a regulation is that definitions are clear, consistent, and predictable. While the definitions of medical diagnostic laboratories in the 2025 Medical Laboratory Regulation appear to be largely consistent with international practices, ambiguities are particularly noticeable in the following areas:<\/span><\/p>\n<ul>\n<li><span style=\"font-size: 16px;\"><strong>R&amp;D laboratories<\/strong>,<\/span><\/li>\n<li><span style=\"font-size: 16px;\"><strong>Reference laboratories<\/strong>,<\/span><\/li>\n<li><span style=\"font-size: 16px;\"><strong>Treatment laboratories<\/strong>,<\/span><\/li>\n<li><span style=\"font-size: 16px;\"><strong>Advanced medical laboratory applications<\/strong>.<\/span><\/li>\n<\/ul>\n<p><span style=\"font-size: 16px;\">For example:<\/span><\/p>\n<ul>\n<li><span style=\"font-size: 16px;\">An organization both <strong>control<\/strong> both <strong>consultancy<\/strong> Having this function could create a risk of conflict of interest.<\/span><\/li>\n<li><span style=\"font-size: 16px;\">Is the criterion of being relevant to human health sufficient on its own to include R&amp;D activities within the scope of clinical diagnostic laboratories?<\/span><\/li>\n<li><span style=\"font-size: 16px;\">Why have the lines between diagnostic, investigative, and therapeutic activities become so blurred?<\/span><\/li>\n<\/ul>\n<p><span style=\"font-size: 16px;\">These questions are not just theoretical; <strong>legal certainty, equality in oversight<\/strong> And <strong>patient safety<\/strong> It is also critically important from that perspective.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"ISO_15189_Perspektifinden_Bakildiginda\"><\/span><span style=\"font-size: 16px;\"><strong>Viewed from the perspective of ISO 15189<\/strong><\/span><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-size: 16px;\">ISO 15189 is a standard specifically developed for medical diagnostic laboratories. Experimental and research laboratories, on the other hand, are evaluated under the &quot;TS EN ISO\/IEC 17025 General Requirements for the Competence of Testing and Calibration Laboratories&quot;.<\/span><\/p>\n<p><span style=\"font-size: 16px;\">The 2025 regulation, however, does not clearly take this distinction into account. It places R&amp;D activities under the same administrative and supervisory framework as diagnostic laboratories, without considering their risk level and purpose.<\/span><\/p>\n<ul>\n<li><span style=\"font-size: 16px;\">A broad interpretation of the limits of authority,<\/span><\/li>\n<li><span style=\"font-size: 16px;\">Purpose-basis incompatibility,<\/span><\/li>\n<li><span style=\"font-size: 16px;\">Divergence from international practices<\/span><\/li>\n<\/ul>\n<p><span style=\"font-size: 16px;\">This brings with it risks.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"Fiziksel_Kriterler_Metrekare_mi_Risk_Temelli_mi\"><\/span><span style=\"font-size: 16px;\"><strong>Physical Criteria: Square Meter or Risk-Based?<\/strong><\/span><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-size: 16px;\">The regulation defines physical areas with detailed square meter definitions. However, international practices define physical infrastructure as follows:<\/span><\/p>\n<ul>\n<li><span style=\"font-size: 16px;\">test type,<\/span><\/li>\n<li><span style=\"font-size: 16px;\">device specifications,<\/span><\/li>\n<li><span style=\"font-size: 16px;\">risk level,<\/span><\/li>\n<li><span style=\"font-size: 16px;\">functional requirements<\/span><\/li>\n<\/ul>\n<p><span style=\"font-size: 16px;\">It considers it accordingly.<\/span><\/p>\n<p><span style=\"font-size: 16px;\">Square meter-based approach:<\/span><\/p>\n<ul>\n<li><span style=\"font-size: 16px;\">It ignores the diversity of laboratories and differences in scale,<\/span><\/li>\n<li><span style=\"font-size: 16px;\">It leads to a significant loss of time and energy during inspections,<\/span><\/li>\n<li><span style=\"font-size: 16px;\">It prioritizes aesthetic conformity over improving quality.<\/span><\/li>\n<\/ul>\n<h3><span class=\"ez-toc-section\" id=\"Personel_ve_Yetkinlik_En_Kritik_Eksik_Alanlardan_Biri\"><\/span><span style=\"font-size: 16px;\"><strong>Personnel and Competence: One of the Most Critical Deficiency Areas<\/strong><\/span><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-size: 16px;\">The regulation defines personnel terms; however, <strong>competence and proficiency<\/strong> It does not adequately address these concepts.<\/span><\/p>\n<p><span style=\"font-size: 16px;\">A person having a specific diploma makes them eligible for that test and that device. <strong>competent<\/strong> This does not mean otherwise. One of the strongest aspects of ISO 15189 is;<\/span><\/p>\n<ul>\n<li><span style=\"font-size: 16px;\">documentation of competence,<\/span><\/li>\n<li><span style=\"font-size: 16px;\">monitoring of performance,<\/span><\/li>\n<li><span style=\"font-size: 16px;\">ensuring continuity<\/span><br \/>\n<span style=\"font-size: 16px;\">It is mandatory.<\/span><\/li>\n<\/ul>\n<p><span style=\"font-size: 16px;\">This deficiency becomes even more apparent in a regulation that specifically emphasizes &quot;advanced technology.&quot;.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"Bilgi_Sistemleri_ve_Dijitallesme_Firsat_mi_Risk_mi\"><\/span><span style=\"font-size: 16px;\"><strong>Information Systems and Digitalization: Opportunity or Risk?<\/strong><\/span><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-size: 16px;\">Information systems, data protection and storage are detailed in the regulation. This is a positive step. However, information systems are not limited to:<\/span><\/p>\n<p><span style=\"font-size: 16px;\">\u201cApproaching it as merely a &quot;record keeping and control tool&quot; carries a serious risk.<\/span><\/p>\n<p><span style=\"font-size: 16px;\">This approach:<\/span><\/p>\n<ul>\n<li><span style=\"font-size: 16px;\">Data integration,<\/span><\/li>\n<li><span style=\"font-size: 16px;\">Traceability,<\/span><\/li>\n<li><span style=\"font-size: 16px;\">Data-driven decision-making,<\/span><\/li>\n<li><span style=\"font-size: 16px;\">The healthy use of artificial intelligence and decision support systems.<\/span><\/li>\n<\/ul>\n<p><span style=\"font-size: 16px;\">long-term limits.<\/span><\/p>\n<p><span style=\"font-size: 16px;\">Information systems are not a technology;, <strong>transformation tool<\/strong> should be considered as such.<\/span><\/p>\n<h3><span class=\"ez-toc-section\" id=\"Sahadan_Gelen_Ses_Anket_Bulgulari_Ne_Diyor\"><\/span><span style=\"font-size: 16px;\"><strong>Voice from the Field: What Do the Survey Findings Say?<\/strong><\/span><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p><span style=\"font-size: 16px;\">An evaluation survey conducted with participants from laboratories of different sizes and types revealed the following perception regarding the regulation:<\/span><\/p>\n<ul>\n<li><span style=\"font-size: 16px;\">Predictability is low.,<\/span><\/li>\n<li><span style=\"font-size: 16px;\">The risk-based approach is weak.,<\/span><\/li>\n<li><span style=\"font-size: 16px;\">Implementation clarity is insufficient.,<\/span><\/li>\n<li>R&amp;D and the transition process are the most problematic areas.<\/li>\n<\/ul>\n<p>The fact that R&amp;D, reference, and advanced technology activities are all handled within the same regulatory framework has been the subject of the most criticism.<\/p>\n<h3><span class=\"ez-toc-section\" id=\"Sonuc_Iyi_Niyet_Iyilestirilmesi_Gereken_Yapisallik\"><\/span><strong>Conclusion: Good Intentions, Structural Issues Needing Improvement<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p>The main objective of the 2025 Medical Laboratory Regulation is... <strong>human health and patient safety<\/strong>This goal is undeniably correct. However, the way to achieve this goal is not through ambiguity, room for interpretation, and formalism;<\/p>\n<ul>\n<li>from clear definitions,<\/li>\n<li>from a risk-based approach,<\/li>\n<li>compliance with international standards,<\/li>\n<li>applicability in the field<\/li>\n<\/ul>\n<p>It is passing.<\/p>\n<p>While the aim is to strengthen patient safety, it is evident that existing regulations need to be structured in a clearer, risk-based, and field-implementable way to support this goal.<\/p>\n<p>The purpose of the interview, the summary of which is presented, is not so much to criticize; <strong>to contribute to improvement<\/strong>. As academics, experts, and field professionals, we are always ready to take responsibility for constructively improving this process.<\/p>\n<p>Kind regards\u2026<\/p>\n<p>Prof. Dr. Diler Aslan<\/p>\n<p>ORCID ID: <a href=\"https:\/\/orcid.org\/0000-0003-4907-9445\">0000-0003-4907-9445<\/a><\/p>\n<p>February 6, 2026<\/p>\n<p><strong>Access to video<\/strong>:<\/p>\n<p><strong>Regulation on Medical Laboratory Services and Advanced Technology Medical Laboratory Applications (Aslan D, S\u00f6zmen E, Eker P.)<\/strong><a href=\"https:\/\/www.youtube.com\/watch?v=DEWkGmvYa9U\">https:\/\/www.youtube.com\/watch?v=DEWkGmvYa9U<\/a>)<\/p>","protected":false},"excerpt":{"rendered":"<p>2025 T\u0131bbi Laboratuvar Y\u00f6netmeli\u011fi Neleri De\u011fi\u015ftiriyor? T\u00fcrkiye\u2019de T\u0131bbi Laboratuvarlar Haziran 2026\u2019ya kadar 2024 T\u0131bbi Laboratuvar Y\u00f6netmeli\u011fine haz\u0131rlan\u0131rken 24 Ekim 2025\u2019te kapsam\u0131 de\u011fi\u015fen yeni y\u00f6netmelik yay\u0131mland\u0131. Yay\u0131mland\u0131\u011f\u0131 g\u00fcn y\u00fcr\u00fcrl\u00fc\u011fe girdi. T\u0131bbi (Klinik) laboratuvarlar haricinde genetik, Ar-Ge laboratuvarlar\u0131, d\u0131\u015f kalite de\u011ferlendirme program sa\u011flay\u0131c\u0131lar\u0131, e\u011fitim veren t\u0131bbi laboratuvarlar da bu hizmete y\u00f6nelik y\u00f6netmelik kapsam\u0131na al\u0131nd\u0131. Bu durum olduk\u00e7a&hellip;<\/p>","protected":false},"author":2,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[63],"tags":[251,252,165,253,250],"post_series":[],"class_list":["post-17797","post","type-post","status-publish","format-standard","hentry","category-blog","tag-medical-laboratory","tag-regulation","tag-tibbi-laboratuvar","tag-turkiye","tag-yonetmelik","entry","no-media"],"_links":{"self":[{"href":"https:\/\/www.d-tek.com.tr\/en\/wp-json\/wp\/v2\/posts\/17797","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.d-tek.com.tr\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.d-tek.com.tr\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.d-tek.com.tr\/en\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.d-tek.com.tr\/en\/wp-json\/wp\/v2\/comments?post=17797"}],"version-history":[{"count":7,"href":"https:\/\/www.d-tek.com.tr\/en\/wp-json\/wp\/v2\/posts\/17797\/revisions"}],"predecessor-version":[{"id":17818,"href":"https:\/\/www.d-tek.com.tr\/en\/wp-json\/wp\/v2\/posts\/17797\/revisions\/17818"}],"wp:attachment":[{"href":"https:\/\/www.d-tek.com.tr\/en\/wp-json\/wp\/v2\/media?parent=17797"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.d-tek.com.tr\/en\/wp-json\/wp\/v2\/categories?post=17797"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.d-tek.com.tr\/en\/wp-json\/wp\/v2\/tags?post=17797"},{"taxonomy":"post_series","embeddable":true,"href":"https:\/\/www.d-tek.com.tr\/en\/wp-json\/wp\/v2\/post_series?post=17797"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}