{"id":6624,"date":"2026-05-27T15:01:07","date_gmt":"2026-05-27T09:31:07","guid":{"rendered":"https:\/\/operonstrategist.com\/?p=6624"},"modified":"2026-05-27T15:01:07","modified_gmt":"2026-05-27T09:31:07","slug":"understanding-the-responsibilities-of-economic-operators-under-the-eu-mdr-2017-745","status":"publish","type":"post","link":"https:\/\/operonstrategist.com\/eg-en\/understanding-the-responsibilities-of-economic-operators-under-the-eu-mdr-2017-745\/","title":{"rendered":"Understanding the Responsibilities of Economic Operators Under the EU MDR 2017\/745"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-post\" data-elementor-id=\"6624\" class=\"elementor elementor-6624\" data-elementor-post-type=\"post\">\n\t\t\t\t<div class=\"elementor-element elementor-element-28564677 e-flex e-con-boxed e-con e-parent\" data-id=\"28564677\" 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-3bd97f5c elementor-widget elementor-widget-heading\" data-id=\"3bd97f5c\" 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\">Understanding the Responsibilities of Economic Operators Under the EU MDR 2017\/745<\/h2>\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-798179d e-flex e-con-boxed e-con e-parent\" data-id=\"798179d\" 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-3a1560b0 e-con-full e-flex e-con e-child\" data-id=\"3a1560b0\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-466ed104 elementor-widget elementor-widget-text-editor\" data-id=\"466ed104\" 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;\">The European Union\u2019s Medical Device Regulation (EU MDR) 2017\/745 has introduced significant changes to how medical devices are regulated across the EU. One of the key aspects of this regulation is the clear definition and enhanced responsibilities of economic operators involved in the medical device supply chain. <\/span><\/p><p><span style=\"font-weight: 400;\">These economic operators include manufacturers, authorized representatives, importers, distributors, and persons responsible for regulatory compliance. Understanding their roles and responsibilities is crucial for ensuring compliance with the MDR and maintaining the safety and performance of medical devices in the European market.<\/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-f058034 e-con-full e-flex e-con e-child\" data-id=\"f058034\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t<div class=\"elementor-element elementor-element-2f2749f8 e-con-full e-flex e-con e-child\" data-id=\"2f2749f8\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-1fb2d57b elementor-widget elementor-widget-heading\" data-id=\"1fb2d57b\" 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\">Contact Us for EU MDR Consultation<\/h4>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-8da7333 elementor-widget elementor-widget-wpforms\" data-id=\"8da7333\" 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\/6624\" data-token=\"ec74508000ccae4945515a950d3da251\" data-token-time=\"1780109621\"><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\" >Text Name Paragraph<\/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-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\/6624\"><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-7c55995b e-flex e-con-boxed e-con e-parent\" data-id=\"7c55995b\" 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-5ea36c87 elementor-widget elementor-widget-heading\" data-id=\"5ea36c87\" 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\">1. Manufacturers<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-14fc952f elementor-widget elementor-widget-text-editor\" data-id=\"14fc952f\" 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;\">Manufacturers are at the core of the medical device lifecycle and bear the primary responsibility for compliance with the MDR. Their obligations include:<\/span><\/p><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Quality and Risk Management: Manufacturers must implement and maintain a <\/span><a href=\"https:\/\/operonstrategist.com\/services\/turnkey-project\/quality-management-system\/\"><span style=\"font-weight: 400;\">quality management system<\/span><\/a><span style=\"font-weight: 400;\"> (QMS) and risk management system that aligns with MDR requirements. These systems must be regularly audited and updated to ensure ongoing compliance.<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Technical Documentation: Manufacturers are required to prepare comprehensive <\/span><span style=\"font-weight: 400;\">technical documentation<\/span><span style=\"font-weight: 400;\"> for each device, including the <\/span><a href=\"https:\/\/operonstrategist.com\/the-creation-of-a-declaration-of-conformity\/\"><span style=\"font-weight: 400;\">EU declaration of conformity<\/span><\/a><span style=\"font-weight: 400;\">. This documentation must be kept up-to-date and made available to competent authorities upon request.<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">EUDAMED Registration: Manufacturers must register their devices in the European database for medical devices (EUDAMED) and provide essential information, including Unique Device Identifiers (UDIs).<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Nonconformity and Corrective Actions: In case of any product nonconformity, manufacturers are obligated to take immediate corrective actions, which may include product recall, to protect patient safety.<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Authorized Representative Appointment: If a manufacturer\u2019s registered place of business is outside the EU, they must appoint an authorized representative within the EU to fulfill their regulatory obligations.<\/span><\/li><\/ul>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-9dbf9ed elementor-widget elementor-widget-heading\" data-id=\"9dbf9ed\" 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\">2. Authorized Representatives<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-e1a7ac4 elementor-widget elementor-widget-text-editor\" data-id=\"e1a7ac4\" 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;\">Authorized representatives act on behalf of non-EU manufacturers to ensure compliance with the MDR. Their key responsibilities include:<\/span><\/p><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Mandated Tasks: The authorized representative must perform tasks outlined in the mandate agreed upon with the manufacturer, such as maintaining copies of technical documentation and the EU declaration of conformity.<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">EUDAMED Registration: Similar to manufacturers, authorized representatives must register with EUDAMED and ensure that all relevant information is up-to-date.<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Corrective Actions: They are also responsible for ensuring that corrective actions are taken in the event of product nonconformity and that these actions are reported to competent authorities.<\/span><\/li><\/ul>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-85d458f elementor-widget elementor-widget-heading\" data-id=\"85d458f\" 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\">3. Importers<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-4faafa1 elementor-widget elementor-widget-text-editor\" data-id=\"4faafa1\" 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;\">Importers play a crucial role in ensuring that only compliant devices enter the EU market. Their responsibilities include:<\/span><\/p><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Documentation Maintenance: Importers must maintain copies of technical documentation and EU conformity assessments and provide them to competent authorities upon request.<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Labeling and Instructions for Use: Importers must ensure that devices are properly labeled and include instructions for use in the appropriate languages as per MDR requirements. The importer\u2019s trade name, place of business, and contact information must also be included on the device labeling or packaging.<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">EUDAMED Registration: Importers must register with EUDAMED and ensure compliance with all necessary requirements.<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Reporting Issues: Importers are responsible for forwarding any complaints or reports of serious incidents to the manufacturer or authorized representative and ensuring that corrective actions are taken.<\/span><\/li><\/ul>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-c38aa90 elementor-widget elementor-widget-heading\" data-id=\"c38aa90\" 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\">4. Distributors<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-5663ae2 elementor-widget elementor-widget-text-editor\" data-id=\"5663ae2\" 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;\">Distributors must verify that devices are compliant before placing them on the market. Their key duties include:<\/span><\/p><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Verification of Compliance: Distributors must ensure that devices carry the <a href=\"https:\/\/operonstrategist.com\/elevateplus\/ce-marking-eu-mdr-ivdr\/\">CE marking<\/a>, are accompanied by the EU declaration of conformity, and have appropriate labeling and instructions for use.<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Storage and Transport: Distributors must adhere to the manufacturer\u2019s requirements for storage and transport to maintain the device\u2019s integrity and safety.<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Corrective Actions and Reporting: They are also responsible for taking corrective actions in the case of nonconformity and reporting any complaints, serious incidents, or device recalls to the manufacturer, authorized representative, and importer.<\/span><\/li><\/ul>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-190591d elementor-widget elementor-widget-heading\" data-id=\"190591d\" 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\">5. Person Responsible for Regulatory Compliance<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-c170751 elementor-widget elementor-widget-text-editor\" data-id=\"c170751\" 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;\">Every manufacturer must appoint at least one person responsible for regulatory compliance (PRRC) within their organization. The PRRC is responsible for:<\/span><\/p><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Ensuring Compliance: The PRRC must ensure that the conformity of the device is maintained in accordance with the QMS under which it is manufactured.<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Technical Documentation and <a href=\"https:\/\/operonstrategist.com\/10-essential-strategies-for-effective-post-market-surveillance-under-eu-mdr\/\">Post-Market Surveillance<\/a>: The PRRC must ensure that technical documentation is kept up-to-date and that post-market surveillance activities are conducted as required by the MDR.<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Incident Reporting: The PRRC is also responsible for ensuring that any serious incidents or field safety corrective actions are reported in a timely manner.<\/span><\/li><\/ul>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-ff55ab5 elementor-widget elementor-widget-heading\" data-id=\"ff55ab5\" 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\">Conclusion:<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-6e1f60c elementor-widget elementor-widget-text-editor\" data-id=\"6e1f60c\" 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;\">The EU MDR 2017\/745 has introduced more stringent requirements for economic operators involved in the medical device supply chain. Each operator\u2014manufacturer, authorized representative, importer, distributor, and person responsible for regulatory compliance\u2014has specific roles and responsibilities that are crucial for maintaining the safety and performance of medical devices in the European market. Compliance with these responsibilities not only ensures adherence to the regulation but also enhances the overall accountability and transparency within the medical device industry.<\/span><\/p><p><i><span style=\"font-weight: 400;\">For more information on navigating the complexities of the EU MDR, or to get professional assistance with regulatory compliance, <\/span><\/i><a href=\"https:\/\/operonstrategist.com\/contact-us\/\"><i><span style=\"font-weight: 400;\">contact Operon Strategist<\/span><\/i><\/a><i><span style=\"font-weight: 400;\">, your trusted <\/span><\/i><a href=\"https:\/\/operonstrategist.com\/services\/regulatory-approvals\/ce-marking\/\"><i><span style=\"font-weight: 400;\">EU MDR consultant<\/span><\/i><\/a><i><span style=\"font-weight: 400;\">. Our team of experts is here to guide you through every step of the process.<\/span><\/i><\/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>The European Union\u2019s Medical Device Regulation (EU MDR) 2017\/745 has introduced significant changes to how medical devices are regulated across the EU. One of the key aspects of this regulation is the clear definition and enhanced responsibilities of economic operators involved in the medical device supply chain. These economic operators include manufacturers, authorized representatives, importers, [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":6738,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[55],"tags":[],"class_list":["post-6624","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\/6624","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=6624"}],"version-history":[{"count":0,"href":"https:\/\/operonstrategist.com\/eg-en\/wp-json\/wp\/v2\/posts\/6624\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/operonstrategist.com\/eg-en\/wp-json\/wp\/v2\/media\/6738"}],"wp:attachment":[{"href":"https:\/\/operonstrategist.com\/eg-en\/wp-json\/wp\/v2\/media?parent=6624"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/operonstrategist.com\/eg-en\/wp-json\/wp\/v2\/categories?post=6624"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/operonstrategist.com\/eg-en\/wp-json\/wp\/v2\/tags?post=6624"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}