1.0hollandbiohttps://www.hollandbio.nl/en/rich600338<blockquote class="wp-embedded-content" data-secret="amDiB0vKoA"><a href="https://www.hollandbio.nl/en/event-en/online-symposium-ctr/">Online-symposium CTR</a></blockquote><iframe sandbox="allow-scripts" security="restricted" src="https://www.hollandbio.nl/en/event-en/online-symposium-ctr/embed/#?secret=amDiB0vKoA" width="600" height="338" title="“Online-symposium CTR” — hollandbio" data-secret="amDiB0vKoA" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"></iframe><script> /*! This file is auto-generated */ !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); //# sourceURL=https://www.hollandbio.nl/wp-includes/js/wp-embed.min.js </script> Op 31 januari 2022 is de European Clinical Trial Regulation (CTR) definitief in werking getreden. Per 31 januari 2023 moeten alle nieuwe studies die onder de CTR vallen via CTIS ingediend worden. Het doel van deze nieuwe wetgeving (CTR) is Europese centralisatie en harmonisatie van toetsingsprocedures voor klinische trials met geneesmiddelen, waarmee de EU aantrekkelijker […]https://dcrfonline.nl/wp-content/uploads/sites/12/2022/12/Plaatje-Bijeenkomst-CTR-17-januari-2023.jpg