{"version":"1.0","provider_name":"LS Academy","provider_url":"https:\/\/lsacademy.site-dev.it\/it\/","author_name":"Francesca Archetti","author_url":"https:\/\/lsacademy.site-dev.it\/it\/author\/francesca-archetti\/","title":"Training Reporting Requirements in Veterinary PhV | LS Academy","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"E3BR5Px1y6\"><a href=\"https:\/\/lsacademy.site-dev.it\/it\/product\/veterinary-pharmacovigilance-and-reporting-requirements\/\">Reporting Requirements in Veterinary Pharmacovigilance<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/lsacademy.site-dev.it\/it\/product\/veterinary-pharmacovigilance-and-reporting-requirements\/embed\/#?secret=E3BR5Px1y6\" width=\"600\" height=\"338\" title=\"&#8220;Reporting Requirements in Veterinary Pharmacovigilance&#8221; &#8212; LS Academy\" data-secret=\"E3BR5Px1y6\" 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","thumbnail_url":"https:\/\/lsacademy.com\/wp-content\/uploads\/2024\/02\/VetPVreporting.jpg","thumbnail_width":1920,"thumbnail_height":1080,"description":"The implementation of adverse event reporting, signal management and the continuous safety evaluation of veterinary medicinal products by trained and competent personnel is one of the essential requirements of the EU pharmacovigilance legislation and the guidelines on good veterinary pharmacovigilance practice. All personnel involved in adverse event reporting and signal management should have received specific &hellip; Continued"}