{"version":"1.0","provider_name":"MEDtech Ingenieur GmbH","provider_url":"https:\/\/medtech-ingenieur.de\/en","author_name":"Goran Madzar","author_url":"https:\/\/medtech-ingenieur.de\/en\/author\/gmadzar\/","title":"FDA Cybersecurity Leitfaden f\u00fcr die Zulassung - MEDtech Ingenieur GmbH","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"Ncl3WWgHZ5\"><a href=\"https:\/\/medtech-ingenieur.de\/en\/fda-cybersecurity-leitfaden-fuer-die-zulassung\/\">FDA Cybersecurity Approval Guidelines<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/medtech-ingenieur.de\/en\/fda-cybersecurity-leitfaden-fuer-die-zulassung\/embed\/#?secret=Ncl3WWgHZ5\" width=\"600\" height=\"338\" title=\"\u201cFDA Cybersecurity Guidance for Regulatory Approval\u201d \u2014 MEDtech Ingenieur GmbH\" data-secret=\"Ncl3WWgHZ5\" 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:\/\/medtech-ingenieur.de\/wp-includes\/js\/wp-embed.min.js\n\/* ]]> *\/\n<\/script>","thumbnail_url":"https:\/\/medtech-ingenieur.de\/wp-content\/uploads\/2021\/03\/checklist-2945401_640.jpg","thumbnail_width":640,"thumbnail_height":426,"description":"Wer ein Medizinprodukt in der USA zulassen will, kommt an der Food and Drug Administration (FDA &#8211; Beh\u00f6rde f\u00fcr Zulassung von Medizinprodukten in der USA) nicht vorbei. Medizinprodukte werden immer vernetzter und erfassen zunehmend mehr Daten. Dabei bleibt es nicht aus, dass Medizinprodukte Ziel von Angreifern werden. Um dem zu begegnen, hat die FDA das [&hellip;]"}