{"version":"1.0","provider_name":"GMED Medical Device Certification","provider_url":"https:\/\/lne-gmed.com\/fr","title":"R\u00e8glement d\u2019ex\u00e9cution (UE) 2025\/2526 : correction et d\u00e9signation des laboratoires de r\u00e9f\u00e9rence de l\u2019UE pour les dispositifs m\u00e9dicaux de diagnostic in vitro - GMED Medical Device Certification","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"DvwWfbyfSo\"><a href=\"https:\/\/lne-gmed.com\/fr\/news\/reglement-dexecution-ue-2025-2526\">R\u00e8glement d\u2019ex\u00e9cution (UE) 2025\/2526 : correction et d\u00e9signation des laboratoires de r\u00e9f\u00e9rence de l\u2019UE pour les dispositifs m\u00e9dicaux de diagnostic in vitro<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/lne-gmed.com\/fr\/news\/reglement-dexecution-ue-2025-2526\/embed#?secret=DvwWfbyfSo\" width=\"600\" height=\"338\" title=\"&#8220;R\u00e8glement d\u2019ex\u00e9cution (UE) 2025\/2526 : correction et d\u00e9signation des laboratoires de r\u00e9f\u00e9rence de l\u2019UE pour les dispositifs m\u00e9dicaux de diagnostic in vitro&#8221; &#8212; GMED Medical Device Certification\" data-secret=\"DvwWfbyfSo\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\" class=\"wp-embedded-content\"><\/iframe><script>\n\/*! This file is auto-generated *\/\n!function(d,l){\"use strict\";l.querySelector&&d.addEventListener&&\"undefined\"!=typeof URL&&(d.wp=d.wp||{},d.wp.receiveEmbedMessage||(d.wp.receiveEmbedMessage=function(e){var t=e.data;if((t||t.secret||t.message||t.value)&&!\/[^a-zA-Z0-9]\/.test(t.secret)){for(var s,r,n,a=l.querySelectorAll('iframe[data-secret=\"'+t.secret+'\"]'),o=l.querySelectorAll('blockquote[data-secret=\"'+t.secret+'\"]'),c=new RegExp(\"^https?:$\",\"i\"),i=0;i<o.length;i++)o[i].style.display=\"none\";for(i=0;i<a.length;i++)s=a[i],e.source===s.contentWindow&&(s.removeAttribute(\"style\"),\"height\"===t.message?(1e3<(r=parseInt(t.value,10))?r=1e3:~~r<200&&(r=200),s.height=r):\"link\"===t.message&&(r=new URL(s.getAttribute(\"src\")),n=new URL(t.value),c.test(n.protocol))&&n.host===r.host&&l.activeElement===s&&(d.top.location.href=t.value))}},d.addEventListener(\"message\",d.wp.receiveEmbedMessage,!1),l.addEventListener(\"DOMContentLoaded\",function(){for(var e,t,s=l.querySelectorAll(\"iframe.wp-embedded-content\"),r=0;r<s.length;r++)(t=(e=s[r]).getAttribute(\"data-secret\"))||(t=Math.random().toString(36).substring(2,12),e.src+=\"#?secret=\"+t,e.setAttribute(\"data-secret\",t)),e.contentWindow.postMessage({message:\"ready\",secret:t},\"*\")},!1)))}(window,document);\n\/\/# sourceURL=https:\/\/lne-gmed.com\/wp-includes\/js\/wp-embed.min.js\n<\/script>\n","description":"Read our article on R\u00e8glement d\u2019ex\u00e9cution (UE) 2025\/2526 : correction et d\u00e9signation des laboratoires de r\u00e9f\u00e9rence de l\u2019UE pour les dispositifs m\u00e9dicaux de diagnostic in vitro and view more articles in our library of regulatory updates, medical device certification information, and other updates in the medical device field."}