{"id":10680,"date":"2026-06-08T16:58:15","date_gmt":"2026-06-08T11:28:15","guid":{"rendered":"https:\/\/operonstrategist.com\/?p=10680"},"modified":"2026-06-08T16:58:15","modified_gmt":"2026-06-08T11:28:15","slug":"understanding-the-impact-of-mdcg-2019-6-rev-5-on-eu-medical-device-manufacturers","status":"publish","type":"post","link":"https:\/\/operonstrategist.com\/us-en\/understanding-the-impact-of-mdcg-2019-6-rev-5-on-eu-medical-device-manufacturers\/","title":{"rendered":"Understanding the Impact of MDCG 2019-6 Rev. 5 on EU Medical Device Manufacturers"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-post\" data-elementor-id=\"10680\" class=\"elementor elementor-10680\" data-elementor-post-type=\"post\">\n\t\t\t\t<div class=\"elementor-element elementor-element-5e1b2e47 e-flex e-con-boxed e-con e-parent\" data-id=\"5e1b2e47\" 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-7878aadc elementor-widget elementor-widget-heading\" data-id=\"7878aadc\" 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\">Understanding the Impact of MDCG 2019-6 Rev. 5 on EU Medical Device Manufacturers<\/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-6b6abb19 e-flex e-con-boxed e-con e-parent\" data-id=\"6b6abb19\" 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-10892a26 e-con-full e-flex e-con e-child\" data-id=\"10892a26\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-402e7a3c elementor-widget elementor-widget-heading\" data-id=\"402e7a3c\" 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\n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-ec26e11 elementor-widget elementor-widget-text-editor\" data-id=\"ec26e11\" 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 regulatory landscape for medical devices in the EU continues to evolve under MDR 2017\/745, posing new challenges for manufacturers. The recent update to MDCG 2019-6 (Rev. 5) aims to provide a more structured framework for interactions between manufacturers and Notified Bodies (NBs). However, leading industry organizations\u2014MedTech Europe, AESGP, Medtech &amp; Pharma Platform Association, and COCIR\u2014have raised concerns about the lack of early clinical strategy discussions in the pre-submission phase.<\/span><\/p><p><span style=\"font-weight: 400;\">Without clear provisions for high-level clinical evidence discussions before submission, manufacturers face continued misalignment with Notified Bodies, leading to delays, additional costs, and regulatory uncertainty.<\/span><\/p><p><span style=\"font-weight: 400;\">In this blog, we analyze the key updates in MDCG 2019-6 Rev. 5, the challenges it presents, and how Operon Strategist can help manufacturers streamline their regulatory compliance process.<\/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-7453a535 e-con-full e-flex e-con e-child\" data-id=\"7453a535\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t<div class=\"elementor-element elementor-element-73342856 e-con-full e-flex e-con e-child\" data-id=\"73342856\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-64942ea2 elementor-widget elementor-widget-heading\" data-id=\"64942ea2\" 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\">Talk to our medical device experts\n<\/h4>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-1a1b7342 elementor-widget elementor-widget-wpforms\" data-id=\"1a1b7342\" 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=\"\/us-en\/wp-json\/wp\/v2\/posts\/10680\" data-token=\"08115cc9be9ad5588cc368d2a2d40326\" data-token-time=\"1781359542\"><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\" >Name Text Phone<\/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 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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\/us-en\/wp-json\/wp\/v2\/posts\/10680\"><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-d88774c e-flex e-con-boxed e-con e-parent\" data-id=\"d88774c\" 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-1efbf13d elementor-widget elementor-widget-heading\" data-id=\"1efbf13d\" 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\">What is MDCG 2019-6 Rev. 5?\n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-10197d65 elementor-widget elementor-widget-text-editor\" data-id=\"10197d65\" 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 Medical Device Coordination Group (MDCG) guidance 2019-6 provides manufacturers with a structured approach to engaging with Notified Bodies under the EU MDR and IVDR. The latest Rev. 5 update includes:<\/span><\/p><p><span style=\"font-weight: 400;\">\u00a0\u2714 A clearer structure for pre-submission interactions<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\u2714 Enhanced guidance on submission timelines and documentation<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\u2714 Emphasis on post-market surveillance (PMS) and vigilance<\/span><\/p><p><span style=\"font-weight: 400;\">However, the industry has identified a major shortcoming\u2014the lack of early-stage clinical strategy discussions, which creates uncertainty for manufacturers in aligning their clinical evaluation strategies with Notified Body expectations.<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-0cc6cb5 elementor-widget elementor-widget-heading\" data-id=\"0cc6cb5\" 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\">Why Industry Leaders Are Concerned\n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-8284d4a elementor-widget elementor-widget-text-editor\" data-id=\"8284d4a\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<h4><span style=\"font-weight: 400;\">1. Absence of Clinical Strategy Discussions in Pre-Submission<\/span><\/h4><p><span style=\"font-weight: 400;\">Manufacturers currently lack opportunities to discuss clinical evaluation strategies with Notified Bodies before submitting their technical documentation. This often results in:<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\ud83d\udd39 Unexpected data requirements during the review process<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\ud83d\udd39 Rejections due to misaligned clinical evidence<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\ud83d\udd39 Delays in market approval<\/span><\/p><h4><span style=\"font-weight: 400;\">2. Innovation at Risk Due to Regulatory Uncertainty<\/span><\/h4><p><span style=\"font-weight: 400;\">Unclear clinical expectations can slow down innovation, particularly affecting startups and small manufacturers. Without structured guidance, companies struggle to develop compliant clinical evaluation plans, increasing the risk of nonconformities.<\/span><\/p><h4><span style=\"font-weight: 400;\">3. Increased Costs &amp; Delays for Manufacturers<\/span><\/h4><p><span style=\"font-weight: 400;\">\ud83d\udd39 Rework of clinical evidence leads to additional testing and trials<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\ud83d\udd39 Extended regulatory timelines increase time-to-market<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\ud83d\udd39 Higher compliance costs impact the feasibility of bringing new devices to market<\/span><\/p><h4><span style=\"font-weight: 400;\">Industry\u2019s Call to Action<\/span><\/h4><p><span style=\"font-weight: 400;\">In their position paper, MedTech Europe, AESGP, Medtech &amp; Pharma Platform Association, and COCIR urge EU policymakers to:<\/span><\/p><p><span style=\"font-weight: 400;\">\u00a0\u2714 Introduce structured clinical strategy discussions before submission<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\u2714 Provide clear clinical evidence guidelines for manufacturers<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\u2714 Align Notified Body requirements across EU Member States<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\u2714 Address these gaps in the upcoming implementing act on Notified Body requirements<\/span><\/p><p><span style=\"font-weight: 400;\">Until regulatory changes are made, manufacturers must take proactive steps to enhance their clinical evidence strategy and ensure compliance with MDR requirements.<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-507e37d elementor-widget elementor-widget-heading\" data-id=\"507e37d\" 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 Medical Device Manufacturers Can Prepare<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-0559ea5 elementor-widget elementor-widget-text-editor\" data-id=\"0559ea5\" 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;\">\u2705 Conduct a Clinical Evidence Gap Analysis<\/span><\/p><p><span style=\"font-weight: 400;\">Identify potential weaknesses in your <\/span><span style=\"font-weight: 400;\">clinical evaluation report<\/span><span style=\"font-weight: 400;\"> (CER) and <\/span><a href=\"https:\/\/operonstrategist.com\/services\/post-market-clinical-follow-up\/\"><span style=\"font-weight: 400;\">post-market clinical follow-up<\/span><\/a><span style=\"font-weight: 400;\"> (PMCF) plan before submission.<\/span><\/p><p><span style=\"font-weight: 400;\">\u2705 Strengthen Technical Documentation<\/span><\/p><p><span style=\"font-weight: 400;\">Ensure all clinical and technical documentation aligns with Notified Body expectations to prevent unnecessary rework and delays.<\/span><\/p><p><span style=\"font-weight: 400;\">\u2705 Engage with Regulatory Experts<\/span><\/p><p><span style=\"font-weight: 400;\">Regulatory consultants can help navigate MDCG guidance and Notified Body expectations, ensuring smooth regulatory approvals.<\/span><\/p><p><span style=\"font-weight: 400;\">\u2705 Implement a Robust Post-Market Surveillance (PMS) Strategy<\/span><\/p><p><span style=\"font-weight: 400;\">A strong <\/span><span style=\"font-weight: 400;\">post-market surveillance<\/span><span style=\"font-weight: 400;\"> and vigilance reporting system enhances compliance and demonstrates commitment to device safety and performance.<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-5b8c404 elementor-widget elementor-widget-text-editor\" data-id=\"5b8c404\" 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>Need Help With Your EU MDR Compliance?<\/strong><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-698b45b elementor-align-center elementor-widget elementor-widget-button\" data-id=\"698b45b\" 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-aa6e8da elementor-widget elementor-widget-heading\" data-id=\"aa6e8da\" 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 Can Help You Navigate EU MDR Compliance\n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-aa20b03 elementor-widget elementor-widget-text-editor\" data-id=\"aa20b03\" 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;\">Getting your medical device approved under the <a href=\"https:\/\/operonstrategist.com\/elevateplus\/ce-marking-eu-mdr-ivdr\/\">EU MDR<\/a> 2017\/745 can feel overwhelming\u2014but you don\u2019t have to do it alone. At Operon Strategist, we\u2019re here to simplify the process and guide you every step of the way.<\/span><\/p><p><span style=\"font-weight: 400;\">Here\u2019s how we can support you:<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\u2705 <\/span><span style=\"font-weight: 400;\">Technical Documentation<\/span><span style=\"font-weight: 400;\"> Made Easy \u2013 We help you prepare MDR-compliant documentation, so you\u2019re always audit-ready.<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\u2705 <\/span><span style=\"font-weight: 400;\">Clinical Evaluation<\/span><span style=\"font-weight: 400;\"> Support \u2013 From CER and PMCF to risk management, we ensure your submissions are rock-solid.<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\u2705 Regulatory Gap Analysis \u2013 We identify and fix compliance gaps before they become roadblocks.<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\u2705 Notified Body Consultation \u2013 Get expert advice on aligning with regulatory expectations and avoiding costly delays.<\/span><\/p><p><span style=\"font-weight: 400;\">With our expertise, you can streamline approvals, cut unnecessary costs, and bring your medical device to market faster. <\/span><a href=\"https:\/\/operonstrategist.com\/contact-us\/\"><span style=\"font-weight: 400;\">Contact us now<\/span><\/a><span style=\"font-weight: 400;\">!<\/span><\/p><p><i><span style=\"font-weight: 400;\">Let\u2019s make MDR compliance smoother\u2014so you can focus on innovation and success<\/span><\/i><span style=\"font-weight: 400;\">!<\/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>Introduction The regulatory landscape for medical devices in the EU continues to evolve under MDR 2017\/745, posing new challenges for manufacturers. The recent update to MDCG 2019-6 (Rev. 5) aims to provide a more structured framework for interactions between manufacturers and Notified Bodies (NBs). However, leading industry organizations\u2014MedTech Europe, AESGP, Medtech &amp; Pharma Platform Association, [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":10681,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[55],"tags":[],"class_list":["post-10680","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-regulatory"],"_links":{"self":[{"href":"https:\/\/operonstrategist.com\/us-en\/wp-json\/wp\/v2\/posts\/10680","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/operonstrategist.com\/us-en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/operonstrategist.com\/us-en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/operonstrategist.com\/us-en\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/operonstrategist.com\/us-en\/wp-json\/wp\/v2\/comments?post=10680"}],"version-history":[{"count":5,"href":"https:\/\/operonstrategist.com\/us-en\/wp-json\/wp\/v2\/posts\/10680\/revisions"}],"predecessor-version":[{"id":10756,"href":"https:\/\/operonstrategist.com\/us-en\/wp-json\/wp\/v2\/posts\/10680\/revisions\/10756"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/operonstrategist.com\/us-en\/wp-json\/wp\/v2\/media\/10681"}],"wp:attachment":[{"href":"https:\/\/operonstrategist.com\/us-en\/wp-json\/wp\/v2\/media?parent=10680"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/operonstrategist.com\/us-en\/wp-json\/wp\/v2\/categories?post=10680"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/operonstrategist.com\/us-en\/wp-json\/wp\/v2\/tags?post=10680"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}