{"version":"1.0","provider_name":"Clinical Services","provider_url":"https:\/\/www.almacgroup.com\/clinical-services","author_name":"amoreland","author_url":"https:\/\/www.almacgroup.com\/clinical-services\/author\/amoreland\/","title":"EU Clinical Trial Regulation: On-Demand Webinar","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"SmG6SKiGIE\"><a href=\"https:\/\/www.almacgroup.com\/clinical-services\/eu-clinical-trial-regulation-on-demand-webinar\/\">EU Clinical Trial Regulation: On-Demand Webinar<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/www.almacgroup.com\/clinical-services\/eu-clinical-trial-regulation-on-demand-webinar\/embed\/#?secret=SmG6SKiGIE\" width=\"600\" height=\"338\" title=\"&#8220;EU Clinical Trial Regulation: On-Demand Webinar&#8221; &#8212; Clinical Services\" data-secret=\"SmG6SKiGIE\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\" class=\"wp-embedded-content\"><\/iframe><script type=\"text\/javascript\">\n\/* <![CDATA[ *\/\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\/* ]]> *\/\n<\/script>\n","description":"Managing your Trials Through Transition and Beyond The new Regulation is fully applicable, Clinical Trials Information System (CTIS) is live, and the EU is progressing quickly through the first of two transition periods from the Clinical Trial Directive to the new Regulation.&nbsp; Sponsors must assess their existing and upcoming trials and consider their plans for [&hellip;]","thumbnail_url":"https:\/\/www.almacgroup.com\/clinical-services\/wp-content\/uploads\/sites\/7\/2020\/11\/Almac_Logo.jpeg","thumbnail_width":640,"thumbnail_height":334}