{"id":6878,"date":"2026-05-30T12:18:59","date_gmt":"2026-05-30T06:48:59","guid":{"rendered":"https:\/\/operonstrategist.com\/?p=6878"},"modified":"2026-05-30T12:18:59","modified_gmt":"2026-05-30T06:48:59","slug":"medical-device-market-entry-eu-vs-us-analysis","status":"publish","type":"post","link":"https:\/\/operonstrategist.com\/dz-en\/medical-device-market-entry-eu-vs-us-analysis\/","title":{"rendered":"Navigating the Medical Device Market Entry Gameplan: The EU and The US Analysis"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-post\" data-elementor-id=\"6878\" class=\"elementor elementor-6878\" data-elementor-post-type=\"post\">\n\t\t\t\t<div class=\"elementor-element elementor-element-705969c9 e-flex e-con-boxed e-con e-parent\" data-id=\"705969c9\" 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-42b11f9c elementor-widget elementor-widget-heading\" data-id=\"42b11f9c\" 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\">Navigating the Medical Device Market Entry Gameplan: The EU and The US Analysis<\/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-2b143ab8 e-flex e-con-boxed e-con e-parent\" data-id=\"2b143ab8\" 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-5aac44bc e-con-full e-flex e-con e-child\" data-id=\"5aac44bc\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-22619728 elementor-widget elementor-widget-heading\" data-id=\"22619728\" 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\">Overview: How to Launch Medical Devices to the Market<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-2d6671fa elementor-widget elementor-widget-text-editor\" data-id=\"2d6671fa\" 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;\">Bringing a medical device to the market is a rigorous process that involves navigating complex regulatory frameworks. In particular, launching medical devices in the European Union (EU) and the United States (US) presents unique challenges and opportunities for manufacturers. Understanding the differences between these two major markets is crucial for successful market entry. In this blog, we\u2019ll explore the key differences in launching medical devices in the EU versus the US.<\/span><\/p><p><a href=\"https:\/\/operonstrategist.com\/services\/turnkey-project\/\"><span style=\"font-weight: 400;\">Get All-in-one Turnkey Project Consulting Services for your medical device launch<\/span><\/a><\/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-2c87aa7f e-con-full e-flex e-con e-child\" data-id=\"2c87aa7f\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t<div class=\"elementor-element elementor-element-775281c0 e-con-full e-flex e-con e-child\" data-id=\"775281c0\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-2fccf887 elementor-widget elementor-widget-heading\" data-id=\"2fccf887\" 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-25c12df6 elementor-widget elementor-widget-wpforms\" data-id=\"25c12df6\" 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=\"\/dz-en\/wp-json\/wp\/v2\/posts\/6878\" data-token=\"ec74508000ccae4945515a950d3da251\" data-token-time=\"1780152338\"><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>\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\" >Phone 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_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><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\/dz-en\/wp-json\/wp\/v2\/posts\/6878\"><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-31587b36 e-flex e-con-boxed e-con e-parent\" data-id=\"31587b36\" 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-be40816 elementor-widget elementor-widget-heading\" data-id=\"be40816\" 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\">Introduction to the EU and the US Medical Device Market\n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-5561deef elementor-widget elementor-widget-text-editor\" data-id=\"5561deef\" 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 medical device market is diverse and strictly regulated by the European Medicines Agency (EMA) and the Medical Device Regulation (MDR). It offers a wide range of products and prioritizes patient safety and quality. Key growth drivers include innovation, an aging population, and rising healthcare spending. The market fosters competition, prompting companies to innovate for improved patient care.<\/span><\/p><p><span style=\"font-weight: 400;\">The US medical device market is globally significant, offering a wide range of products that meet stringent FDA regulations for safety and efficacy. Technological advancements, an aging population, and rising chronic diseases drive market growth, while competition spurs continual innovation to enhance patient outcomes.<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-29a5181 elementor-widget elementor-widget-heading\" data-id=\"29a5181\" 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\">Consideration of Choosing the First Medical Device Market to Enter<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-4c04c54 elementor-widget elementor-widget-text-editor\" data-id=\"4c04c54\" 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;\">Choosing the first market to enter as a medical device manufacturer involves weighing several factors. Here\u2019s a concise breakdown of key considerations for entering the European Union (EU) or the United States (US):<\/span><\/p><ol><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Regulatory Environment:<\/span><ul><li style=\"font-weight: 400;\" aria-level=\"1\">EU: Governed by the Medical Device Regulation (MDR), requiring <a href=\"https:\/\/operonstrategist.com\/services\/regulatory-approvals\/ce-marking\/\"><span>CE marking<\/span><\/a><span>.<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\">US: The US FDA oversees regulations under the Federal Food, Drug, and Cosmetic Act, including premarket notification (<a href=\"https:\/\/operonstrategist.com\/services\/regulatory-approvals\/fda-510k\/\"><span>FDA 510(k)<\/span><\/a><span>), premarket approval (PMA), and other pathways.<\/span><\/li><\/ul><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Market Size and Growth Potential:<\/span><ul><li style=\"font-weight: 400;\" aria-level=\"1\">US: Largest global market with high healthcare spending and demand for innovation.<\/li><li style=\"font-weight: 400;\" aria-level=\"1\">EU: Diverse market with over 450 million people, offering substantial growth potential.<\/li><\/ul><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Market Access and Entry Barriers:<\/span><ul><li style=\"font-weight: 400;\" aria-level=\"1\">EU: A single regulatory framework streamlines access but obtaining CE marking can be time-consuming.<\/li><li style=\"font-weight: 400;\" aria-level=\"1\">US: The FDA clearance or approval process can be lengthy and rigorous.<\/li><\/ul><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Competitive Landscape and Market Dynamics:<\/span><ul><li style=\"font-weight: 400;\" aria-level=\"1\">US: Highly competitive with established players and startups; differentiation crucial.<\/li><li style=\"font-weight: 400;\" aria-level=\"1\">EU: Competitive mix of companies; understanding market dynamics essential.<\/li><\/ul><\/li><\/ol>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-03784ce elementor-widget elementor-widget-heading\" data-id=\"03784ce\" 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\">Regulatory Frameworks as per Medical Device Market\n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-4498516 elementor-widget elementor-widget-text-editor\" data-id=\"4498516\" 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;\">European Union (EU):<\/span><\/p><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">The EU operates under the Medical Device Regulation (MDR) framework, which replaced the previous Medical Device Directive (MDD) in May 2021. The MDR aims to enhance patient safety and streamline the regulatory process for medical devices.<\/span><ul><li style=\"font-weight: 400;\" aria-level=\"2\"><span style=\"font-weight: 400;\">Under the MDR, medical devices are classified into four risk categories: Class I, IIa, IIb, and III, based on their intended use and potential risks.<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"2\"><span style=\"font-weight: 400;\">Manufacturers must obtain <\/span><a href=\"https:\/\/operonstrategist.com\/services\/regulatory-approvals\/ce-marking\/\"><span style=\"font-weight: 400;\">CE marking,<\/span><\/a><span style=\"font-weight: 400;\"> indicating conformity with EU regulations, before placing their devices on the market.<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"2\"><span style=\"font-weight: 400;\">The MDR emphasizes post-market surveillance and increased transparency, requiring manufacturers to provide more comprehensive clinical data and undergo stricter conformity assessments.<br \/><\/span>\u00a0\u00a0<\/li><\/ul><\/li><\/ul><p><span style=\"font-weight: 400;\">United States (US):<\/span><\/p><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">In the US, medical devices are regulated by the Food and Drug Administration (FDA) under the Federal Food, Drug, and Cosmetic Act (FD&amp;C Act) and the Medical Device Regulation Act (MDRA).<\/span><ul><li style=\"font-weight: 400;\" aria-level=\"2\"><span style=\"font-weight: 400;\">The FDA classifies medical devices into three categories: Class I, II, and III, based on risk and level of regulatory control.<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"2\"><span style=\"font-weight: 400;\">Most Class I devices are exempt from premarket notification (<\/span><a href=\"https:\/\/operonstrategist.com\/services\/regulatory-approvals\/fda-510k\/\"><span style=\"font-weight: 400;\">FDA 510(k)<\/span><\/a><span style=\"font-weight: 400;\">) or premarket approval (PMA) requirements, while Class II and III devices typically require FDA clearance or approval before marketing.<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"2\"><span style=\"font-weight: 400;\">The FDA emphasizes a risk-based approach, focusing regulatory scrutiny on higher-risk devices while facilitating expedited pathways for innovative technologies through programs like the Breakthrough Devices Program and the De Novo pathway.<\/span><\/li><\/ul><\/li><\/ul><p><span style=\"font-weight: 400;\">Read <\/span><a href=\"https:\/\/operonstrategist.com\/ce-mark-vs-fda-approval-for-medical-devices\/\"><span style=\"font-weight: 400;\">CE Mark vs FDA Approval For Medical Devices<\/span><\/a><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-f85cb3b elementor-widget elementor-widget-heading\" data-id=\"f85cb3b\" 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\">Key Differences\n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-55c567e elementor-widget elementor-widget-text-editor\" data-id=\"55c567e\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Regulatory Pathways:<\/span><\/li><\/ul><p><span style=\"font-weight: 400;\">\u2013 EU\u2019s CE marking process: centralized and predictable.<\/span><\/p><p><span style=\"font-weight: 400;\">\u2013 FDA\u2019s pathways: variable and complex, especially PMA for Class III devices.<\/span><\/p><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Clinical Evidence Requirements:<\/span><\/li><\/ul><p><span style=\"font-weight: 400;\">\u2013 MDR emphasizes robust clinical data, including PMCF studies.<\/span><\/p><p><span style=\"font-weight: 400;\">\u2013 The FDA accepts well-designed trials or real-world evidence for higher-risk devices.<\/span><\/p><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Market Access and Timelines:<\/span><\/li><\/ul><p><span style=\"font-weight: 400;\">\u2013 The CE marking process in the EU can be time-consuming.<\/span><\/p><p><span style=\"font-weight: 400;\">\u2013 The FDA offers expedited review pathways like Priority Review and Breakthrough Devices Program in the US.<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-b16eebf elementor-widget elementor-widget-text-editor\" data-id=\"b16eebf\" 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>Globalize Your Medical Device: Seamlessly Launch Anywhere with Operon Strategist&#8217;s Expertise!<\/strong><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-5a69cd8 elementor-align-center elementor-widget elementor-widget-button\" data-id=\"5a69cd8\" 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\">Contact 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-ce40413 elementor-widget elementor-widget-text-editor\" data-id=\"ce40413\" 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;\">Operon Strategist plays a pivotal role in guiding medical device manufacturers through the complexities of launching their products in the EU and US markets. With their regulatory expertise, strategic planning capabilities, and commitment to streamlining market access, Operon Strategist empowers clients to navigate regulatory hurdles with confidence and achieve successful market entry.<\/span><\/p><p><br \/><br \/><\/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>Overview: How to Launch Medical Devices to the Market Bringing a medical device to the market is a rigorous process that involves navigating complex regulatory frameworks. In particular, launching medical devices in the European Union (EU) and the United States (US) presents unique challenges and opportunities for manufacturers. Understanding the differences between these two major [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":6879,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[55],"tags":[],"class_list":["post-6878","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-regulatory"],"_links":{"self":[{"href":"https:\/\/operonstrategist.com\/dz-en\/wp-json\/wp\/v2\/posts\/6878","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/operonstrategist.com\/dz-en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/operonstrategist.com\/dz-en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/operonstrategist.com\/dz-en\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/operonstrategist.com\/dz-en\/wp-json\/wp\/v2\/comments?post=6878"}],"version-history":[{"count":0,"href":"https:\/\/operonstrategist.com\/dz-en\/wp-json\/wp\/v2\/posts\/6878\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/operonstrategist.com\/dz-en\/wp-json\/wp\/v2\/media\/6879"}],"wp:attachment":[{"href":"https:\/\/operonstrategist.com\/dz-en\/wp-json\/wp\/v2\/media?parent=6878"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/operonstrategist.com\/dz-en\/wp-json\/wp\/v2\/categories?post=6878"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/operonstrategist.com\/dz-en\/wp-json\/wp\/v2\/tags?post=6878"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}