{"id":15467,"date":"2026-06-22T15:21:14","date_gmt":"2026-06-22T09:51:14","guid":{"rendered":"https:\/\/operonstrategist.com\/?p=15467"},"modified":"2026-06-22T15:21:14","modified_gmt":"2026-06-22T09:51:14","slug":"10-key-steps-to-achieve-eu-ai-act-compliance-for-medical-device","status":"publish","type":"post","link":"https:\/\/operonstrategist.com\/eg-en\/10-key-steps-to-achieve-eu-ai-act-compliance-for-medical-device\/","title":{"rendered":"EU AI Act Compliance: Understanding the AI Act and Its Impact on Healthcare"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-post\" data-elementor-id=\"15467\" class=\"elementor elementor-15467\" data-elementor-post-type=\"post\">\n\t\t\t\t<div class=\"elementor-element elementor-element-300498ff e-flex e-con-boxed e-con e-parent\" data-id=\"300498ff\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-6f4e2d52 elementor-widget elementor-widget-heading\" data-id=\"6f4e2d52\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h1 class=\"elementor-heading-title elementor-size-default\">EU AI Act Compliance: Understanding the AI Act and Its Impact on Healthcare<\/h1>\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-7bbdb956 e-flex e-con-boxed e-con e-parent\" data-id=\"7bbdb956\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t<div class=\"elementor-element elementor-element-250daad2 e-con-full e-flex e-con e-child\" data-id=\"250daad2\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-4aeb4246 elementor-widget elementor-widget-text-editor\" data-id=\"4aeb4246\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p>\u00a0<\/p><p><span style=\"font-weight: 400;\">EU AI Act compliance marks a monumental shift in how artificial intelligence is regulated across industries, especially in healthcare. As of August 1, 2024, the European Union\u2019s AI Act became the first comprehensive regulation aimed at governing AI technologies globally. This new regulation establishes a unified framework for all 27 EU member states, ensuring fair competition and consistent standards for businesses operating within the EU.\u00a0<\/span><\/p><p><span style=\"font-weight: 400;\">For the healthcare sector, the AI Act carries specific significance. Many AI applications used in medical devices are classified as high-risk, meaning they face more stringent regulatory requirements. Healthcare organizations must carefully assess their AI systems to ensure they meet safety, transparency, and human oversight standards as mandated by the EU AI Act. <\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-98d577e e-con-full e-flex e-con e-child\" data-id=\"98d577e\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t<div class=\"elementor-element elementor-element-35647983 e-con-full e-flex e-con e-child\" data-id=\"35647983\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-58b4d2f2 elementor-widget elementor-widget-heading\" data-id=\"58b4d2f2\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h4 class=\"elementor-heading-title elementor-size-default\">Regulatory Excellence for Global Medical Device Markets\n<\/h4>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-7afa31dd elementor-widget elementor-widget-wpforms\" data-id=\"7afa31dd\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"wpforms.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<div class=\"wpforms-container wpforms-container-full wpforms-render-modern\" id=\"wpforms-6203\"><form id=\"wpforms-form-6203\" class=\"wpforms-validate wpforms-form wpforms-ajax-form\" data-formid=\"6203\" method=\"post\" enctype=\"multipart\/form-data\" action=\"\/eg-en\/wp-json\/wp\/v2\/posts\/15467\" data-token=\"bb0d01854beaa56b1f74d7cc9636528a\" data-token-time=\"1782139911\"><noscript class=\"wpforms-error-noscript\">Please enable JavaScript in your browser to complete this form.<\/noscript><div id=\"wpforms-error-noscript\" style=\"display: none;\">Please enable JavaScript in your browser to complete this form.<\/div><div class=\"wpforms-field-container\"><div id=\"wpforms-6203-field_1-container\" class=\"wpforms-field wpforms-field-name\" data-field-id=\"1\"><label class=\"wpforms-field-label wpforms-label-hide\" for=\"wpforms-6203-field_1\" aria-hidden=\"false\">Name <span class=\"wpforms-required-label\" aria-hidden=\"true\">*<\/span><\/label><input type=\"text\" id=\"wpforms-6203-field_1\" class=\"wpforms-field-large wpforms-field-required\" name=\"wpforms[fields][1]\" placeholder=\"Name*\" aria-errormessage=\"wpforms-6203-field_1-error\" required><\/div><div id=\"wpforms-6203-field_2-container\" class=\"wpforms-field wpforms-field-email\" data-field-id=\"2\"><label class=\"wpforms-field-label wpforms-label-hide\" for=\"wpforms-6203-field_2\" aria-hidden=\"false\">Email <span class=\"wpforms-required-label\" aria-hidden=\"true\">*<\/span><\/label><input type=\"email\" id=\"wpforms-6203-field_2\" class=\"wpforms-field-large wpforms-field-required\" name=\"wpforms[fields][2]\" placeholder=\"Email*\" spellcheck=\"false\" aria-errormessage=\"wpforms-6203-field_2-error\" required><\/div>\t\t<div id=\"wpforms-6203-field_5-container\"\n\t\t\tclass=\"wpforms-field wpforms-field-text\"\n\t\t\tdata-field-type=\"text\"\n\t\t\tdata-field-id=\"5\"\n\t\t\t>\n\t\t\t<label class=\"wpforms-field-label\" for=\"wpforms-6203-field_5\" >Paragraph Name Email<\/label>\n\t\t\t<input type=\"text\" id=\"wpforms-6203-field_5\" class=\"wpforms-field-medium\" name=\"wpforms[fields][5]\" >\n\t\t<\/div>\n\t\t<div id=\"wpforms-6203-field_3-container\" class=\"wpforms-field wpforms-field-phone\" data-field-id=\"3\"><label class=\"wpforms-field-label wpforms-label-hide\" for=\"wpforms-6203-field_3\" aria-hidden=\"false\">Phone <span class=\"wpforms-required-label\" aria-hidden=\"true\">*<\/span><\/label><input type=\"tel\" id=\"wpforms-6203-field_3\" class=\"wpforms-field-large wpforms-field-required wpforms-smart-phone-field\" data-rule-smart-phone-field=\"true\" name=\"wpforms[fields][3]\" placeholder=\"Phone*\" aria-label=\"Phone\" aria-errormessage=\"wpforms-6203-field_3-error\" required><\/div><div id=\"wpforms-6203-field_4-container\" class=\"wpforms-field wpforms-field-textarea\" data-field-id=\"4\"><label class=\"wpforms-field-label wpforms-label-hide\" for=\"wpforms-6203-field_4\" aria-hidden=\"false\">Paragraph Text <span class=\"wpforms-required-label\" aria-hidden=\"true\">*<\/span><\/label><textarea id=\"wpforms-6203-field_4\" class=\"wpforms-field-medium wpforms-field-required\" name=\"wpforms[fields][4]\" placeholder=\"Message\" aria-errormessage=\"wpforms-6203-field_4-error\" required><\/textarea><\/div><script>\n\t\t\t\t( function() {\n\t\t\t\t\tconst style = document.createElement( 'style' );\n\t\t\t\t\tstyle.appendChild( document.createTextNode( '#wpforms-6203-field_5-container { position: absolute !important; overflow: hidden !important; display: inline !important; height: 1px !important; width: 1px !important; z-index: -1000 !important; padding: 0 !important; } #wpforms-6203-field_5-container input { visibility: hidden; } #wpforms-conversational-form-page #wpforms-6203-field_5-container label { counter-increment: none; }' ) );\n\t\t\t\t\tdocument.head.appendChild( style );\n\t\t\t\t\tdocument.currentScript?.remove();\n\t\t\t\t} )();\n\t\t\t<\/script><\/div><!-- .wpforms-field-container --><div class=\"wpforms-recaptcha-container wpforms-is-recaptcha wpforms-is-recaptcha-type-v3\" ><input type=\"hidden\" name=\"wpforms[recaptcha]\" value=\"\"><\/div><div class=\"wpforms-submit-container\" ><input type=\"hidden\" name=\"wpforms[id]\" value=\"6203\"><input type=\"hidden\" name=\"page_title\" value=\"\"><input type=\"hidden\" name=\"page_url\" value=\"https:\/\/operonstrategist.com\/eg-en\/wp-json\/wp\/v2\/posts\/15467\"><input type=\"hidden\" name=\"url_referer\" value=\"\"><button type=\"submit\" name=\"wpforms[submit]\" id=\"wpforms-submit-6203\" class=\"wpforms-submit\" data-alt-text=\"Sending...\" data-submit-text=\"Submit\" aria-live=\"assertive\" value=\"wpforms-submit\">Submit<\/button><img decoding=\"async\" src=\"https:\/\/operonstrategist.com\/wp-content\/plugins\/wpforms\/assets\/images\/submit-spin.svg\" class=\"wpforms-submit-spinner\" style=\"display: none;\" width=\"26\" height=\"26\" alt=\"Loading\"><\/div><\/form><\/div>  <!-- .wpforms-container -->\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-7f0783a e-flex e-con-boxed e-con e-parent\" data-id=\"7f0783a\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-7f8888a2 elementor-widget elementor-widget-heading\" data-id=\"7f8888a2\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">10 Key Steps to Achieve EU AI Act Compliance for Healthcare Providers<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-b64a09b elementor-widget elementor-widget-text-editor\" data-id=\"b64a09b\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<ol><li style=\"font-weight: 400;\" aria-level=\"1\"><strong>Assess Your AI Systems<\/strong><span style=\"font-weight: 400;\"> \u2013 First, determine whether your medical devices include AI\/ML technologies. If so, classify these systems as \u201chigh-risk\u201d under the EU AI Act and prepare them for registration in the EU\u2019s high-risk AI system database.\u00a0<br \/><br \/><\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><strong>Implement an AI <a href=\"https:\/\/operonstrategist.com\/services\/turnkey-project\/quality-management-system\/\">Quality Management System (QMS)<\/a><\/strong><span style=\"font-weight: 400;\"> \u2013 Adapt your existing medical device QMS to include AI-specific requirements. Ensure alignment with Article 17 of the EU AI Act and consider integrating it with <\/span><a href=\"https:\/\/operonstrategist.com\/services\/turnkey-project\/quality-management-system\/iso-13485\/\"><span style=\"font-weight: 400;\">ISO\/IEC 13485<\/span><\/a><span style=\"font-weight: 400;\">, which is the standard for medical device quality management.\u00a0<br \/><br \/><\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><strong>Create Comprehensive <a href=\"https:\/\/operonstrategist.com\/medical-device-technical-documentation-for-mdr\/\">Technical Documentation<\/a><\/strong><span style=\"font-weight: 400;\"> \u2013 Ensure you develop detailed documentation for your AI systems as outlined in Annex IV of the Act. This should cover system design, data requirements, training methods, and performance metrics, all while syncing with existing EU MDR\/IVDR documentation.\u00a0<br \/><br \/><\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><strong>Establish a Robust <a href=\"https:\/\/operonstrategist.com\/medical-device-risk-management\/\">Risk Management System<\/a><\/strong><span style=\"font-weight: 400;\"> \u2013 Identify, evaluate, and mitigate AI-related risks. This should be integrated with the risk management practices from the EU MDR to address potential health, safety, and human rights concerns.\u00a0<br \/><br \/><\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><strong>Strengthen Your Data Governance<\/strong><span style=\"font-weight: 400;\"> \u2013 Assess the quality, availability, and bias of the datasets used in your AI systems. Consider factors such as geographical location, behavioral patterns, and context to ensure your data is unbiased and reliable.\u00a0<br \/><br \/><\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><strong>Focus on Transparency and Human Oversight<\/strong><span style=\"font-weight: 400;\"> \u2013 Transparency is a key requirement under the EU AI Act. Make sure your AI systems are transparent, and establish robust human oversight mechanisms to ensure accountability.\u00a0<br \/><br \/><\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><strong>Set Up Incident Reporting and Ongoing Monitoring<\/strong><span style=\"font-weight: 400;\"> \u2013 Develop a system to report AI-related incidents and ensure continuous post-market monitoring of your AI systems to track their performance and address any issues that arise.\u00a0<br \/><br \/><\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><strong>Conduct Fundamental Rights Impact Assessments<\/strong><span style=\"font-weight: 400;\"> \u2013 Evaluate the potential impacts of your AI systems on fundamental rights, and take necessary steps to mitigate any risks identified during this process.\u00a0<br \/><br \/><\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><strong>Designate an EU Authorized Representative<\/strong><span style=\"font-weight: 400;\"> \u2013 If your business is based outside the EU, it is mandatory to appoint an authorized representative to handle EU AI Act compliance on your behalf.\u00a0<br \/><br \/><\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><strong>Prepare for <a href=\"https:\/\/operonstrategist.com\/conformity-assessment-procedures-for-medical-devices-under-eu-mdr-2017-745\/\">Conformity Assessment<\/a><\/strong><span style=\"font-weight: 400;\"> \u2013 Conduct internal assessments to ensure your AI systems meet the regulatory requirements. Work with notified bodies for certification, particularly for high-risk systems, ensuring compliance with both MDR\/IVDR and the EU AI Act.<\/span><\/li><\/ol>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-2e6644c elementor-widget elementor-widget-text-editor\" data-id=\"2e6644c\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><strong>Want to Know More On EU AI Act Compliance?<\/strong><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-83413bf elementor-align-center elementor-widget elementor-widget-button\" data-id=\"83413bf\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"button.default\">\n\t\t\t\t\t\t\t\t\t\t<a class=\"elementor-button elementor-button-link elementor-size-sm\" href=\"https:\/\/operonstrategist.com\/contact-us\/\">\n\t\t\t\t\t\t<span class=\"elementor-button-content-wrapper\">\n\t\t\t\t\t\t\t\t\t<span class=\"elementor-button-text\">Connect with Us!<\/span>\n\t\t\t\t\t<\/span>\n\t\t\t\t\t<\/a>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-be5c49d elementor-widget elementor-widget-heading\" data-id=\"be5c49d\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">How Operon Strategist Helps with EU AI Act Compliance\n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-351b05b elementor-widget elementor-widget-text-editor\" data-id=\"351b05b\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">As a trusted name in regulatory consulting, Operon Strategist plays a pivotal role in helping manufacturers navigate the complexities of PSUR preparation and compliance.\u00a0\u00a0<\/span><\/p><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\"><strong>Expert Guidance<\/strong>: Operon Strategist ensures clarity in understanding and implementing the MDR requirements, reducing the burden on manufacturers.\u00a0\u00a0<\/span><\/li><\/ul><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\"><strong>Streamlined Processes<\/strong>: The team assists in organizing and presenting PSUR data effectively, adhering to all nine compliance rules.\u00a0\u00a0<\/span><\/li><\/ul><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\"><strong>Risk Mitigation<\/strong>: With Operon\u2019s strategic support, manufacturers can proactively address compliance gaps and minimize regulatory risks.\u00a0\u00a0<\/span><\/li><\/ul><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\"><strong>Comprehensive Solutions<\/strong>: Operon\u2019s expertise extends across a wide range of devices, offering tailored solutions for both legacy and MDR-compliant products.\u00a0<br \/><br \/><\/span><\/li><\/ul><p><span style=\"font-weight: 400;\">Operon Strategist delivers complete solutions for obtaining <\/span><a href=\"https:\/\/operonstrategist.com\/services\/\"><span style=\"font-weight: 400;\">regulatory approvals<\/span><\/a><span style=\"font-weight: 400;\">, including <\/span><a href=\"https:\/\/operonstrategist.com\/services\/regulatory-approvals\/ce-marking\/\"><span style=\"font-weight: 400;\">European CE Marking<\/span><\/a><span style=\"font-weight: 400;\">, <\/span><a href=\"https:\/\/operonstrategist.com\/elevateplus\/us-fda-510k-qmsr-registration\/\"><span style=\"font-weight: 400;\">FDA 510(k)<\/span><\/a><span style=\"font-weight: 400;\">, <\/span><a href=\"https:\/\/operonstrategist.com\/services\/regulatory-approvals\/cdsco-registration\/cdsco-import-license\/\"><span style=\"font-weight: 400;\">Indian CDSCO Import Registration<\/span><\/a><span style=\"font-weight: 400;\">, <\/span><a href=\"https:\/\/operonstrategist.com\/services\/regulatory-approvals\/medical-device-registration-in-saudi-arabia\/\"><span style=\"font-weight: 400;\">SFDA<\/span><\/a><span style=\"font-weight: 400;\">, and <\/span><a href=\"https:\/\/operonstrategist.com\/elevateplus\/ukca-marking\/\"><span style=\"font-weight: 400;\">UKCA compliance<\/span><\/a><span style=\"font-weight: 400;\">. We also support the establishment of manufacturing facilities by offering services such as <\/span><a href=\"https:\/\/operonstrategist.com\/services\/turnkey-project\/manufacturing-facility\/\"><span style=\"font-weight: 400;\">facility layout design<\/span><\/a><span style=\"font-weight: 400;\">, <\/span><a href=\"https:\/\/operonstrategist.com\/services\/turnkey-project\/clean-room-guidance\/\"><span style=\"font-weight: 400;\">cleanroom planning<\/span><\/a><span style=\"font-weight: 400;\">, <\/span><a href=\"https:\/\/operonstrategist.com\/services\/turnkey-project\/validation-doc\/\"><span style=\"font-weight: 400;\">machine validation<\/span><\/a><span style=\"font-weight: 400;\">, and ensuring facility adherence to global regulatory standards ensuring quality through ISO 13485, <\/span><span style=\"font-weight: 400;\">FDA QSR<\/span><span style=\"font-weight: 400;\"> and <\/span><a href=\"https:\/\/operonstrategist.com\/services\/turnkey-project\/quality-management-system\/mdsap\/\"><span style=\"font-weight: 400;\">MDSAP<\/span><\/a><span style=\"font-weight: 400;\"> compliance and all regulatory approvals.\u00a0<\/span><\/p><p><span style=\"font-weight: 400;\">By choosing Operon Strategist, manufacturers gain a reliable partner dedicated to ensuring regulatory success and market readiness. Their proactive approach transforms challenges into opportunities, empowering businesses to thrive in the global medical device market.\u00a0<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>EU AI Act compliance marks a monumental shift in how artificial intelligence is regulated across industries, especially in healthcare. As of August 1, 2024, the European Union\u2019s AI Act became the first comprehensive regulation aimed at governing AI technologies globally. This new regulation establishes a unified framework for all 27 EU member states, ensuring fair [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":15530,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[55],"tags":[],"class_list":["post-15467","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-regulatory"],"_links":{"self":[{"href":"https:\/\/operonstrategist.com\/eg-en\/wp-json\/wp\/v2\/posts\/15467","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/operonstrategist.com\/eg-en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/operonstrategist.com\/eg-en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/operonstrategist.com\/eg-en\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/operonstrategist.com\/eg-en\/wp-json\/wp\/v2\/comments?post=15467"}],"version-history":[{"count":1,"href":"https:\/\/operonstrategist.com\/eg-en\/wp-json\/wp\/v2\/posts\/15467\/revisions"}],"predecessor-version":[{"id":15531,"href":"https:\/\/operonstrategist.com\/eg-en\/wp-json\/wp\/v2\/posts\/15467\/revisions\/15531"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/operonstrategist.com\/eg-en\/wp-json\/wp\/v2\/media\/15530"}],"wp:attachment":[{"href":"https:\/\/operonstrategist.com\/eg-en\/wp-json\/wp\/v2\/media?parent=15467"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/operonstrategist.com\/eg-en\/wp-json\/wp\/v2\/categories?post=15467"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/operonstrategist.com\/eg-en\/wp-json\/wp\/v2\/tags?post=15467"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}