{"version":"1.0","provider_name":"MPR China Certification GmbH","provider_url":"https:\/\/www.china-certification.com\/en\/","author_name":"Julian Busch","author_url":"https:\/\/www.china-certification.com\/en\/author\/julian-busch\/","title":"CFDA: Priority Review Procedure for Medical Devices - MPR China Certification GmbH","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"hTXzZNo2bp\"><a href=\"https:\/\/www.china-certification.com\/en\/cfda-priority-review-procedure-for-medical-devices\/\">CFDA: Priority Review Procedure for Medical Devices<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/www.china-certification.com\/en\/cfda-priority-review-procedure-for-medical-devices\/embed\/#?secret=hTXzZNo2bp\" width=\"600\" height=\"338\" title=\"&#8220;CFDA: Priority Review Procedure for Medical Devices&#8221; &#8212; MPR China Certification GmbH\" data-secret=\"hTXzZNo2bp\" 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\/\/# sourceURL=https:\/\/www.china-certification.com\/wp-includes\/js\/wp-embed.min.js\n\/* ]]> *\/\n<\/script>\n","description":"The China Food and Drug Administration (CFDA) issued a draft of regulation for priority review for medical device manufacturers. The circular proposes the qualifying criteria, process and features of the priority review. The public was able to comment the draft until July 20th 2016. In China it is necessary that manufacturers of class II and [&hellip;]"}