{"version":"1.0","provider_name":"Team Consulting","provider_url":"https:\/\/team-consulting.hostings.co.uk\/us","author_name":"Margaux Lesaffre","author_url":"https:\/\/team-consulting.hostings.co.uk\/us\/author\/margaux-lesaffre\/","title":"Medical device regulation - Team Consulting","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"V4P2nBuKDn\"><a href=\"https:\/\/team-consulting.hostings.co.uk\/us\/insights\/medical-device-regulation\/\">Medical device regulation<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/team-consulting.hostings.co.uk\/us\/insights\/medical-device-regulation\/embed\/#?secret=V4P2nBuKDn\" width=\"600\" height=\"338\" title=\"&#8220;Medical device regulation&#8221; &#8212; Team Consulting\" data-secret=\"V4P2nBuKDn\" 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:\/\/team-consulting.hostings.co.uk\/us\/wp-includes\/js\/wp-embed.min.js\n<\/script>\n","thumbnail_url":"https:\/\/teamconsulting-cdn-1.s3.eu-west-2.amazonaws.com\/wp-content\/uploads\/2021\/06\/24124659\/feature-img-6.jpg","thumbnail_width":270,"thumbnail_height":230,"description":"Brought about at least in part by the PIP silicone implant scandal of the late 1990s and early 2000s, the overhaul of the European medical device regulations which resulted in the introduction of the MDR (Medical Device Regulation) has been underway for many years. As an engineer working in medical device development I find it [&hellip;]"}