{"id":7216,"date":"2024-02-05T10:00:46","date_gmt":"2024-02-05T08:00:46","guid":{"rendered":"https:\/\/eu.bd.com\/iv-news\/?p=7216"},"modified":"2024-03-07T09:15:25","modified_gmt":"2024-03-07T08:15:25","slug":"key-insights-on-recent-amendments-to-eu-mdr","status":"publish","type":"post","link":"https:\/\/eu.bd.com\/iv-news\/news-innovation\/key-insights-on-recent-amendments-to-eu-mdr\/","title":{"rendered":"Key insights on recent amendments to EU-MDR"},"content":{"rendered":"<p>The European Medical Device Regulation (EU-MDR) 2017\/745 has brought many changes to the medical device industry and product availability. Thanks to the EU-MDR, product offerings are becoming more streamlined, addressing clinician preferences and hospital needs with quality, value and utility. Learn more about the history of the EU-MDR and its recent amendments.<\/p>\n<h2>Brief history of the EU-MDR<\/h2>\n<p>The MDR came into force on 26th May 2017 and became applicable on 26th May 2021 in all EU member states. This regulation has replaced the Medical Device Directive (MDD) and sets reinforced rules for applying the \u2018CE\u2019 mark to medical devices.<\/p>\n<p><b><span data-contrast=\"none\">More on this topic: <\/span><\/b><a href=\"https:\/\/eu.bd.com\/iv-news\/news-innovation\/preventing-sharps-injuries-european-biosafety-network-publishes-new-guidance\/\">Preventing sharps injuries \u2013 European Biosafety Network publishes new guidance<\/a><\/p>\n<h3>The regulation aims to bring about significant improvements to the MDD system. The reinforced rules bring:<sup>1<\/sup><\/h3>\n<ul>\n<li><strong>S<\/strong><strong>tricter previous control for high-risk devices<\/strong> with the involvement of a pool of experts at the EU level<\/li>\n<li><strong>The reinforcement of the criteria for designation and processes for oversight of notified bodies<\/strong><\/li>\n<li><strong>The inclusion of aesthetic devices <\/strong>under the scope of the regulation<\/li>\n<li><strong>Improved transparency <\/strong>through a comprehensive EU database on medical devices and a device traceability system based on a unique device identification<\/li>\n<li><strong>The introduction of an \u2018implant card\u2019 <\/strong>for patients containing information about implanted medical devices<\/li>\n<li><strong>The reinforcement of the rules on clinical evidence<\/strong>, including an EU-wide coordinated procedure for authorising multi-centre clinical investigations<\/li>\n<li><strong>The strengthening of post-market surveillance <\/strong>requirements for manufacturers<\/li>\n<li><strong>Improved coordination mechanisms <\/strong>between EU countries in the fields of vigilance and market surveillance<\/li>\n<\/ul>\n<h2>Why is the EU-MDR important?<\/h2>\n<p>The EU-MDR aims to ensure the smooth functioning of the internal market as regards medical devices, taking as a base a high level of protection of the health of patients and users.<\/p>\n<p>The regulation also sets high standards of quality and safety for medical devices to meet common safety concerns by ensuring, among other things, that the data generated in clinical investigations are reliable and robust and that the safety of the subjects participating in a clinical investigation is protected.<\/p>\n<p><b><span data-contrast=\"none\">More on this topic: <\/span><\/b><a href=\"https:\/\/eu.bd.com\/iv-news\/news-innovation\/skin-antiseptics-now-categorised-as-medicinal-products-what-the-new-aemps-regulatory-framework-entails\/https:\/\/eu.bd.com\/iv-news\/news-innovation\/skin-antiseptics-now-categorised-as-medicinal-products-what-the-new-aemps-regulatory-framework-entails\/\">Skin antiseptics now categorised as medicinal products: What the new AEMPS regulatory framework entails<\/a><\/p>\n<h2>Recent EU-MDR amendments<\/h2>\n<h3>Though it comes with many changes, ensuring the highest quality of safety and quality in medical devices is likely to lead to clinical efficiencies, including:<\/h3>\n<ul>\n<li>Less training time<sup>2<\/sup><\/li>\n<li>Improved product familiarity<sup>3<\/sup><\/li>\n<li>Fewer errors<sup>4<\/sup><\/li>\n<li>More time to focus on patient care<sup>5<\/sup><\/li>\n<\/ul>\n<p>Since taking effect in May 2021, the EU-MDR has included <a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/EN\/TXT\/?uri=CELEX:32023R0607\">regulation (EU) 2023\/607<\/a>, updating the transition period until the end of December 2027 for class III and class IIb implantable devices, with a few exceptions.<sup>6 <\/sup>For class IIb implantable devices not covered above, class IIa devices and for class I devices placed on the market in sterile condition or having a measuring function, the transition period has been updated until the end of December 2028.<sup>6<\/sup><\/p>\n<p><strong>Learn more about the impact of the EU-MDR and its recent amendments:<\/strong><\/p>\n<div class=\"su-button-center\"><a href=\"https:\/\/eu.bd.com\/iv-news\/wp-content\/uploads\/2024\/01\/BD-54156-EU-MDR-Overview-Brochure-and-FAQ-2023.12.18-APPROVED.pdf\" class=\"su-button su-button-style-default\" style=\"color:#FFFFFF;background-color:#2D89EF;border-color:#246ec0;border-radius:6px\" target=\"_blank\" rel=\"noopener noreferrer\"><span style=\"color:#FFFFFF;padding:0px 18px;font-size:14px;line-height:28px;border-color:#6cadf4;border-radius:6px;text-shadow:none\"> LEARN MORE ABOUT EU-MDR<\/span><\/a><\/div>\n","protected":false},"excerpt":{"rendered":"<p>The European Medical Device Regulation (EU-MDR) 2017\/745 has brought many changes to the medical device industry and product availability. Thanks&#8230;<\/p>\n","protected":false},"author":8,"featured_media":7219,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[1],"tags":[],"class_list":["post-7216","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-news-innovation","speciality-critical-care-emergency-care","speciality-healthcare-worker-safety","speciality-patient-safety","contenttype-article","target-doctor","target-hospital-director-manager","target-procurement"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Key insights on recent amendments to EU-MDR - BD IV News<\/title>\n<meta name=\"description\" content=\"Learn more about the recent amendments to the European Union&#039;s European Medical Device Regulation (EU-MDR) 2017\/745.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/eu.bd.com\/iv-news\/news-innovation\/key-insights-on-recent-amendments-to-eu-mdr\/\" \/>\n<meta property=\"og:locale\" content=\"en_GB\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Key insights on recent amendments to EU-MDR - BD IV News\" \/>\n<meta property=\"og:description\" content=\"Learn more about the recent amendments to the European Union&#039;s European Medical Device Regulation (EU-MDR) 2017\/745.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/eu.bd.com\/iv-news\/news-innovation\/key-insights-on-recent-amendments-to-eu-mdr\/\" \/>\n<meta property=\"og:site_name\" content=\"BD IV News\" \/>\n<meta property=\"article:published_time\" content=\"2024-02-05T08:00:46+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2024-03-07T08:15:25+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/eu.bd.com\/iv-news\/wp-content\/uploads\/2024\/01\/Emerald_syringe_EU-MDR.jpg\" \/>\n\t<meta property=\"og:image:width\" content=\"994\" \/>\n\t<meta property=\"og:image:height\" content=\"424\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/jpeg\" \/>\n<meta name=\"author\" content=\"Camille Suarez\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Camille Suarez\" \/>\n\t<meta name=\"twitter:label2\" content=\"Estimated reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"3 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/news-innovation\\\/key-insights-on-recent-amendments-to-eu-mdr\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/news-innovation\\\/key-insights-on-recent-amendments-to-eu-mdr\\\/\"},\"author\":{\"name\":\"Camille Suarez\",\"@id\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/#\\\/schema\\\/person\\\/133274b3c3f2b1e2a25492760340ccf2\"},\"headline\":\"Key insights on recent amendments to EU-MDR\",\"datePublished\":\"2024-02-05T08:00:46+00:00\",\"dateModified\":\"2024-03-07T08:15:25+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/news-innovation\\\/key-insights-on-recent-amendments-to-eu-mdr\\\/\"},\"wordCount\":505,\"publisher\":{\"@id\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/#organization\"},\"image\":{\"@id\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/news-innovation\\\/key-insights-on-recent-amendments-to-eu-mdr\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/wp-content\\\/uploads\\\/2024\\\/01\\\/Emerald_syringe_EU-MDR.jpg\",\"articleSection\":[\"News and innovation\"],\"inLanguage\":\"en-GB\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/news-innovation\\\/key-insights-on-recent-amendments-to-eu-mdr\\\/\",\"url\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/news-innovation\\\/key-insights-on-recent-amendments-to-eu-mdr\\\/\",\"name\":\"Key insights on recent amendments to EU-MDR - BD IV News\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/#website\"},\"primaryImageOfPage\":{\"@id\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/news-innovation\\\/key-insights-on-recent-amendments-to-eu-mdr\\\/#primaryimage\"},\"image\":{\"@id\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/news-innovation\\\/key-insights-on-recent-amendments-to-eu-mdr\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/wp-content\\\/uploads\\\/2024\\\/01\\\/Emerald_syringe_EU-MDR.jpg\",\"datePublished\":\"2024-02-05T08:00:46+00:00\",\"dateModified\":\"2024-03-07T08:15:25+00:00\",\"description\":\"Learn more about the recent amendments to the European Union's European Medical Device Regulation (EU-MDR) 2017\\\/745.\",\"inLanguage\":\"en-GB\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/news-innovation\\\/key-insights-on-recent-amendments-to-eu-mdr\\\/\"]}]},{\"@type\":\"ImageObject\",\"inLanguage\":\"en-GB\",\"@id\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/news-innovation\\\/key-insights-on-recent-amendments-to-eu-mdr\\\/#primaryimage\",\"url\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/wp-content\\\/uploads\\\/2024\\\/01\\\/Emerald_syringe_EU-MDR.jpg\",\"contentUrl\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/wp-content\\\/uploads\\\/2024\\\/01\\\/Emerald_syringe_EU-MDR.jpg\",\"width\":994,\"height\":424,\"caption\":\"A healthcare worker treating a patient with a device regulated by the EU-MDR.\"},{\"@type\":\"WebSite\",\"@id\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/#website\",\"url\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/\",\"name\":\"BD IV News\",\"description\":\"Your source of information on intravenous therapy, medication delivery and vascular access management.\",\"publisher\":{\"@id\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-GB\"},{\"@type\":\"Organization\",\"@id\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/#organization\",\"name\":\"BD IV News\",\"url\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/\",\"logo\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-GB\",\"@id\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/#\\\/schema\\\/logo\\\/image\\\/\",\"url\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/wp-content\\\/uploads\\\/2024\\\/04\\\/BD-Master-Logo-on-Warm-White-512X512px.png\",\"contentUrl\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/wp-content\\\/uploads\\\/2024\\\/04\\\/BD-Master-Logo-on-Warm-White-512X512px.png\",\"width\":512,\"height\":512,\"caption\":\"BD IV News\"},\"image\":{\"@id\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/#\\\/schema\\\/logo\\\/image\\\/\"}},{\"@type\":\"Person\",\"@id\":\"https:\\\/\\\/eu.bd.com\\\/iv-news\\\/#\\\/schema\\\/person\\\/133274b3c3f2b1e2a25492760340ccf2\",\"name\":\"Camille Suarez\",\"image\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-GB\",\"@id\":\"https:\\\/\\\/secure.gravatar.com\\\/avatar\\\/f50a86470bf0edfb5227a77db11a6f6ab98f270489a78660886c4d7bf008f2bd?s=96&d=mm&r=g\",\"url\":\"https:\\\/\\\/secure.gravatar.com\\\/avatar\\\/f50a86470bf0edfb5227a77db11a6f6ab98f270489a78660886c4d7bf008f2bd?s=96&d=mm&r=g\",\"contentUrl\":\"https:\\\/\\\/secure.gravatar.com\\\/avatar\\\/f50a86470bf0edfb5227a77db11a6f6ab98f270489a78660886c4d7bf008f2bd?s=96&d=mm&r=g\",\"caption\":\"Camille Suarez\"}}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Key insights on recent amendments to EU-MDR - BD IV News","description":"Learn more about the recent amendments to the European Union's European Medical Device Regulation (EU-MDR) 2017\/745.","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/eu.bd.com\/iv-news\/news-innovation\/key-insights-on-recent-amendments-to-eu-mdr\/","og_locale":"en_GB","og_type":"article","og_title":"Key insights on recent amendments to EU-MDR - BD IV News","og_description":"Learn more about the recent amendments to the European Union's European Medical Device Regulation (EU-MDR) 2017\/745.","og_url":"https:\/\/eu.bd.com\/iv-news\/news-innovation\/key-insights-on-recent-amendments-to-eu-mdr\/","og_site_name":"BD IV News","article_published_time":"2024-02-05T08:00:46+00:00","article_modified_time":"2024-03-07T08:15:25+00:00","og_image":[{"width":994,"height":424,"url":"https:\/\/eu.bd.com\/iv-news\/wp-content\/uploads\/2024\/01\/Emerald_syringe_EU-MDR.jpg","type":"image\/jpeg"}],"author":"Camille Suarez","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Camille Suarez","Estimated reading time":"3 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/eu.bd.com\/iv-news\/news-innovation\/key-insights-on-recent-amendments-to-eu-mdr\/#article","isPartOf":{"@id":"https:\/\/eu.bd.com\/iv-news\/news-innovation\/key-insights-on-recent-amendments-to-eu-mdr\/"},"author":{"name":"Camille Suarez","@id":"https:\/\/eu.bd.com\/iv-news\/#\/schema\/person\/133274b3c3f2b1e2a25492760340ccf2"},"headline":"Key insights on recent amendments to EU-MDR","datePublished":"2024-02-05T08:00:46+00:00","dateModified":"2024-03-07T08:15:25+00:00","mainEntityOfPage":{"@id":"https:\/\/eu.bd.com\/iv-news\/news-innovation\/key-insights-on-recent-amendments-to-eu-mdr\/"},"wordCount":505,"publisher":{"@id":"https:\/\/eu.bd.com\/iv-news\/#organization"},"image":{"@id":"https:\/\/eu.bd.com\/iv-news\/news-innovation\/key-insights-on-recent-amendments-to-eu-mdr\/#primaryimage"},"thumbnailUrl":"https:\/\/eu.bd.com\/iv-news\/wp-content\/uploads\/2024\/01\/Emerald_syringe_EU-MDR.jpg","articleSection":["News and innovation"],"inLanguage":"en-GB"},{"@type":"WebPage","@id":"https:\/\/eu.bd.com\/iv-news\/news-innovation\/key-insights-on-recent-amendments-to-eu-mdr\/","url":"https:\/\/eu.bd.com\/iv-news\/news-innovation\/key-insights-on-recent-amendments-to-eu-mdr\/","name":"Key insights on recent amendments to EU-MDR - BD IV News","isPartOf":{"@id":"https:\/\/eu.bd.com\/iv-news\/#website"},"primaryImageOfPage":{"@id":"https:\/\/eu.bd.com\/iv-news\/news-innovation\/key-insights-on-recent-amendments-to-eu-mdr\/#primaryimage"},"image":{"@id":"https:\/\/eu.bd.com\/iv-news\/news-innovation\/key-insights-on-recent-amendments-to-eu-mdr\/#primaryimage"},"thumbnailUrl":"https:\/\/eu.bd.com\/iv-news\/wp-content\/uploads\/2024\/01\/Emerald_syringe_EU-MDR.jpg","datePublished":"2024-02-05T08:00:46+00:00","dateModified":"2024-03-07T08:15:25+00:00","description":"Learn more about the recent amendments to the European Union's European Medical Device Regulation (EU-MDR) 2017\/745.","inLanguage":"en-GB","potentialAction":[{"@type":"ReadAction","target":["https:\/\/eu.bd.com\/iv-news\/news-innovation\/key-insights-on-recent-amendments-to-eu-mdr\/"]}]},{"@type":"ImageObject","inLanguage":"en-GB","@id":"https:\/\/eu.bd.com\/iv-news\/news-innovation\/key-insights-on-recent-amendments-to-eu-mdr\/#primaryimage","url":"https:\/\/eu.bd.com\/iv-news\/wp-content\/uploads\/2024\/01\/Emerald_syringe_EU-MDR.jpg","contentUrl":"https:\/\/eu.bd.com\/iv-news\/wp-content\/uploads\/2024\/01\/Emerald_syringe_EU-MDR.jpg","width":994,"height":424,"caption":"A healthcare worker treating a patient with a device regulated by the EU-MDR."},{"@type":"WebSite","@id":"https:\/\/eu.bd.com\/iv-news\/#website","url":"https:\/\/eu.bd.com\/iv-news\/","name":"BD IV News","description":"Your source of information on intravenous therapy, medication delivery and vascular access management.","publisher":{"@id":"https:\/\/eu.bd.com\/iv-news\/#organization"},"potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/eu.bd.com\/iv-news\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"en-GB"},{"@type":"Organization","@id":"https:\/\/eu.bd.com\/iv-news\/#organization","name":"BD IV News","url":"https:\/\/eu.bd.com\/iv-news\/","logo":{"@type":"ImageObject","inLanguage":"en-GB","@id":"https:\/\/eu.bd.com\/iv-news\/#\/schema\/logo\/image\/","url":"https:\/\/eu.bd.com\/iv-news\/wp-content\/uploads\/2024\/04\/BD-Master-Logo-on-Warm-White-512X512px.png","contentUrl":"https:\/\/eu.bd.com\/iv-news\/wp-content\/uploads\/2024\/04\/BD-Master-Logo-on-Warm-White-512X512px.png","width":512,"height":512,"caption":"BD IV News"},"image":{"@id":"https:\/\/eu.bd.com\/iv-news\/#\/schema\/logo\/image\/"}},{"@type":"Person","@id":"https:\/\/eu.bd.com\/iv-news\/#\/schema\/person\/133274b3c3f2b1e2a25492760340ccf2","name":"Camille Suarez","image":{"@type":"ImageObject","inLanguage":"en-GB","@id":"https:\/\/secure.gravatar.com\/avatar\/f50a86470bf0edfb5227a77db11a6f6ab98f270489a78660886c4d7bf008f2bd?s=96&d=mm&r=g","url":"https:\/\/secure.gravatar.com\/avatar\/f50a86470bf0edfb5227a77db11a6f6ab98f270489a78660886c4d7bf008f2bd?s=96&d=mm&r=g","contentUrl":"https:\/\/secure.gravatar.com\/avatar\/f50a86470bf0edfb5227a77db11a6f6ab98f270489a78660886c4d7bf008f2bd?s=96&d=mm&r=g","caption":"Camille Suarez"}}]}},"lang":"en","translations":{"en":7216,"fr":7275,"de":7305,"it":7322},"pll_sync_post":[],"_links":{"self":[{"href":"https:\/\/eu.bd.com\/iv-news\/wp-json\/wp\/v2\/posts\/7216","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/eu.bd.com\/iv-news\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/eu.bd.com\/iv-news\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/eu.bd.com\/iv-news\/wp-json\/wp\/v2\/users\/8"}],"replies":[{"embeddable":true,"href":"https:\/\/eu.bd.com\/iv-news\/wp-json\/wp\/v2\/comments?post=7216"}],"version-history":[{"count":3,"href":"https:\/\/eu.bd.com\/iv-news\/wp-json\/wp\/v2\/posts\/7216\/revisions"}],"predecessor-version":[{"id":7222,"href":"https:\/\/eu.bd.com\/iv-news\/wp-json\/wp\/v2\/posts\/7216\/revisions\/7222"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/eu.bd.com\/iv-news\/wp-json\/wp\/v2\/media\/7219"}],"wp:attachment":[{"href":"https:\/\/eu.bd.com\/iv-news\/wp-json\/wp\/v2\/media?parent=7216"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/eu.bd.com\/iv-news\/wp-json\/wp\/v2\/categories?post=7216"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/eu.bd.com\/iv-news\/wp-json\/wp\/v2\/tags?post=7216"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}