{"id":162,"date":"2023-04-20T10:43:45","date_gmt":"2023-04-20T08:43:45","guid":{"rendered":"https:\/\/ceiso.fr\/en\/?page_id=162"},"modified":"2023-07-08T16:07:43","modified_gmt":"2023-07-08T14:07:43","slug":"quality-regulatory-trainings","status":"publish","type":"page","link":"https:\/\/ceiso.fr\/en\/quality-regulatory-trainings\/","title":{"rendered":"Quality-Regulatory trainings"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-page\" data-elementor-id=\"162\" class=\"elementor elementor-162\">\n\t\t\t\t\t\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-1cb4db0 elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"1cb4db0\" data-element_type=\"section\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-50 elementor-top-column elementor-element elementor-element-858bb83\" data-id=\"858bb83\" data-element_type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t\t\t<div class=\"elementor-element elementor-element-a144887 elementor-widget elementor-widget-heading\" data-id=\"a144887\" data-element_type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<style>\/*! elementor - v3.12.2 - 23-04-2023 *\/\n.elementor-heading-title{padding:0;margin:0;line-height:1}.elementor-widget-heading .elementor-heading-title[class*=elementor-size-]>a{color:inherit;font-size:inherit;line-height:inherit}.elementor-widget-heading .elementor-heading-title.elementor-size-small{font-size:15px}.elementor-widget-heading .elementor-heading-title.elementor-size-medium{font-size:19px}.elementor-widget-heading .elementor-heading-title.elementor-size-large{font-size:29px}.elementor-widget-heading .elementor-heading-title.elementor-size-xl{font-size:39px}.elementor-widget-heading .elementor-heading-title.elementor-size-xxl{font-size:59px}<\/style><h1 class=\"elementor-heading-title elementor-size-default\">Discover our Quality-Regulatory training catalog<\/h1>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-6197ce8 elementor-widget elementor-widget-text-editor\" data-id=\"6197ce8\" data-element_type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<style>\/*! elementor - v3.12.2 - 23-04-2023 *\/\n.elementor-widget-text-editor.elementor-drop-cap-view-stacked .elementor-drop-cap{background-color:#69727d;color:#fff}.elementor-widget-text-editor.elementor-drop-cap-view-framed .elementor-drop-cap{color:#69727d;border:3px solid;background-color:transparent}.elementor-widget-text-editor:not(.elementor-drop-cap-view-default) .elementor-drop-cap{margin-top:8px}.elementor-widget-text-editor:not(.elementor-drop-cap-view-default) .elementor-drop-cap-letter{width:1em;height:1em}.elementor-widget-text-editor .elementor-drop-cap{float:left;text-align:center;line-height:1;font-size:50px}.elementor-widget-text-editor .elementor-drop-cap-letter{display:inline-block}<\/style>\t\t\t\t<p>You work in a demanding regulatory and normative environment. Your employees\u2019 efficiency is an essential part of your company&#8217;s performance. We support the development and maintenance of your teams\u2019 skills.<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-a2e9b6c elementor-widget elementor-widget-image\" data-id=\"a2e9b6c\" data-element_type=\"widget\" data-widget_type=\"image.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<style>\/*! elementor - v3.12.2 - 23-04-2023 *\/\n.elementor-widget-image{text-align:center}.elementor-widget-image a{display:inline-block}.elementor-widget-image a img[src$=\".svg\"]{width:48px}.elementor-widget-image img{vertical-align:middle;display:inline-block}<\/style>\t\t\t\t\t\t\t\t\t\t\t\t<img decoding=\"async\" width=\"800\" height=\"448\" src=\"https:\/\/ceiso.fr\/en\/wp-content\/uploads\/sites\/2\/2023\/04\/CEISO-Qualiopi-1024x574.png\" class=\"attachment-large size-large wp-image-23\" alt=\"\" loading=\"lazy\" srcset=\"https:\/\/ceiso.fr\/en\/wp-content\/uploads\/sites\/2\/2023\/04\/CEISO-Qualiopi-1024x574.png 1024w, https:\/\/ceiso.fr\/en\/wp-content\/uploads\/sites\/2\/2023\/04\/CEISO-Qualiopi-300x168.png 300w, https:\/\/ceiso.fr\/en\/wp-content\/uploads\/sites\/2\/2023\/04\/CEISO-Qualiopi-768x430.png 768w, https:\/\/ceiso.fr\/en\/wp-content\/uploads\/sites\/2\/2023\/04\/CEISO-Qualiopi-1536x860.png 1536w, https:\/\/ceiso.fr\/en\/wp-content\/uploads\/sites\/2\/2023\/04\/CEISO-Qualiopi.png 1571w\" sizes=\"(max-width: 800px) 100vw, 800px\" \/>\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-0d9ca59 elementor-widget elementor-widget-html\" data-id=\"0d9ca59\" data-element_type=\"widget\" data-widget_type=\"html.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<div class=\"btn-container\">\n<a href=\"#catalogue\" class=\"btn-full\">See the catalog <\/a>\n<a href=\"#calendrier\" class=\"btn-empty\">See the schedule <\/a>\n<\/div>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t<div class=\"elementor-column elementor-col-50 elementor-top-column elementor-element elementor-element-8d8a844\" data-id=\"8d8a844\" data-element_type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t\t\t<div class=\"elementor-element elementor-element-41f7318 elementor-widget elementor-widget-image\" data-id=\"41f7318\" data-element_type=\"widget\" data-widget_type=\"image.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<img decoding=\"async\" width=\"800\" height=\"482\" src=\"https:\/\/ceiso.fr\/en\/wp-content\/uploads\/sites\/2\/2023\/04\/CEISO-formations-Qualite-reglementaire-1024x617.png\" class=\"attachment-large size-large wp-image-164\" alt=\"\" loading=\"lazy\" srcset=\"https:\/\/ceiso.fr\/en\/wp-content\/uploads\/sites\/2\/2023\/04\/CEISO-formations-Qualite-reglementaire-1024x617.png 1024w, https:\/\/ceiso.fr\/en\/wp-content\/uploads\/sites\/2\/2023\/04\/CEISO-formations-Qualite-reglementaire-300x181.png 300w, https:\/\/ceiso.fr\/en\/wp-content\/uploads\/sites\/2\/2023\/04\/CEISO-formations-Qualite-reglementaire-768x463.png 768w, https:\/\/ceiso.fr\/en\/wp-content\/uploads\/sites\/2\/2023\/04\/CEISO-formations-Qualite-reglementaire-1536x925.png 1536w, https:\/\/ceiso.fr\/en\/wp-content\/uploads\/sites\/2\/2023\/04\/CEISO-formations-Qualite-reglementaire-2048x1234.png 2048w\" sizes=\"(max-width: 800px) 100vw, 800px\" \/>\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-9b3b80a elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"9b3b80a\" data-element_type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-a8cabe3\" data-id=\"a8cabe3\" data-element_type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t\t\t<div class=\"elementor-element elementor-element-7e23ae9 elementor-widget elementor-widget-heading\" data-id=\"7e23ae9\" data-element_type=\"widget\" id=\"calendrier\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">Information and training schedule<\/h2>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-968d988 elementor-widget elementor-widget-text-editor\" data-id=\"968d988\" data-element_type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<p>All our trainings courses can be carried out either INTER or INTRA, in-person or in a virtual classroom. We can also design tailor-made training courses to meet your needs.<\/p><p><a class=\"cta-devis\" href=\"https:\/\/ceiso.fr\/en\/contact\/\">Contact us<\/a><\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-257b419 elementor-widget elementor-widget-html\" data-id=\"257b419\" data-element_type=\"widget\" data-widget_type=\"html.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<script>\nwindow.onload = function() {\n  const table = document.getElementById(\"tablepress-formations-q-r\");\n  const filter = document.getElementById(\"filter-table\");\n\nfilter.addEventListener(\"change\", function() {\n  const filterValue = this.value;\n  for (let i = 1; i < table.rows.length; i++) {\n    const row = table.rows[i];\n    const cellValue = row.cells[1].textContent;\n    if (cellValue.toLowerCase().includes(filterValue.toLowerCase()) || filterValue === \"\") {\n      row.style.display = \"\";\n    } else {\n      row.style.display = \"none\";\n    }\n  }\n});\n};\n<\/script>\n\n<select id=\"filter-table\">\n  <option value=\"\">Select a subcategory<\/option>\n  <option value=\"Processes\">Processes<\/option>\n  <option value=\"Quality\">Quality<\/option>\n  <option value=\"International Regulations\">International Regulations<\/option>\n  <option value=\"European Regulations\"> European Regulations<\/option>\n  <option value=\"Risks\">Risks<\/option>\n<\/select>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-ab15323 elementor-widget elementor-widget-text-editor\" data-id=\"ab15323\" data-element_type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<p>*IP = In-person \/ Virt. = Virtual Class\u00a0<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-959a8e3 elementor-widget elementor-widget-shortcode\" data-id=\"959a8e3\" data-element_type=\"widget\" data-widget_type=\"shortcode.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<div class=\"elementor-shortcode\"><div id=\"tablepress-formations-q-r-wrapper\">\n\n<table id=\"tablepress-formations-q-r\" class=\"tablepress tablepress-id-formations-q-r\">\n<thead>\n<tr class=\"row-1 odd\">\n\t<th class=\"column-1\">Training<\/th><th class=\"column-2\">Ref.<\/th><th class=\"column-3\">Duration<\/th><th class=\"column-4\">Price excl. taxes INTER (\u20ac)<\/th><th class=\"column-5\">Jan. 23<\/th><th class=\"column-6\">Feb. 23<\/th><th class=\"column-7\">Mar. 23<\/th><th class=\"column-8\">Apr. 23<\/th><th class=\"column-9\">May 23<\/th><th class=\"column-10\">Jun. 23<\/th><th class=\"column-11\">Jul. 23<\/th>\n<\/tr>\n<\/thead>\n<tbody class=\"row-hover\">\n<tr class=\"row-2 even\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/gr02-medical-devices-risk-management\/\">Medical Devices: Risk Management<\/a><\/td><td class=\"column-2\">Risks - GR02<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\">21\/02 - IP<br \/>\nFULL<\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\">04\/05 - IP. Orsay<\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-3 odd\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/gr03-medical-device-software-development\/\">Medical Device Software Development<\/a><\/td><td class=\"column-2\">Risks - GR03<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-4 even\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/gr04-safety-and-essential-performance-requirements-for-medical-electrical-equipment-en-60601-1\/\">Safety and Essential Performance Requirements for Medical Electrical Equipment \u2013 EN 60601-1<\/a><\/td><td class=\"column-2\">Risks - GR04<\/td><td class=\"column-3\">1,5 days<br \/>\n10,5 hours<\/td><td class=\"column-4\">1200,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-5 odd\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/gr05-application-of-usability-engineering\/\">Application of Usability Engineering<\/a><\/td><td class=\"column-2\">Risks - GR05<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\">08\/06 - IP. Orsay<br \/>\nFULL<\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-6 even\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/gr06-biological-evaluation-of-medical-devices-according-to-en-iso-10993-1\/\">Biological Evaluation of Medical Devices according to EN ISO 10993-1<\/a><\/td><td class=\"column-2\">Risks - GR06<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-7 odd\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq03-quality-management-system-for-medical-devices\/\">Quality Management System for Medical Devices<\/a><\/td><td class=\"column-2\">Quality - MQ03<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\">13\/01 - IP.<br \/>\nFULL<\/td><td class=\"column-6\">09_15 - IP.<br \/>\nFULL<\/td><td class=\"column-7\">30\/03 - IP. Orsay<\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-8 even\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq05-quality-audits-according-to-iso-19011\/\">Quality Audits according to ISO 19011<\/a><\/td><td class=\"column-2\">Quality - MQ05<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\">18\/01 - IP.<br \/>\nFULL<\/td><td class=\"column-6\">23\/02 - IP.<br \/>\nFULL<\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\">17\/05 - IP.<br \/>\nFULL<\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-9 odd\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq06-validation-of-processes-applied-to-medical-devices-and-in-vitro-diagnostic-medical-devices\/\">Validation of Processes applied to Medical Devices and In Vitro Diagnostic Medical Devices<\/a><\/td><td class=\"column-2\">Quality - MQ06<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-10 even\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq10-validation-of-software-applications\/\">Validation of Software Applications<\/a><\/td><td class=\"column-2\">Quality - MQ10<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-11 odd\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl08-compliance-with-us-market-authorization-requirements-for-medical-devices-510k-submission\/\">Compliance with US Market Authorization Requirements for Medical Devices \u2013 510(k) Submission<\/a><\/td><td class=\"column-2\">International Regulations - RL08<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-12 even\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl07-medical-devicesrl15-european-materiovigilance-requirements\/\">Medical Devices: European Materiovigilance Requirements<\/a><\/td><td class=\"column-2\">European Regulations - RL07<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-13 odd\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl12-medical-device-regulation-eu-2017-745-introduction-to-the-regulation\/\">Medical Device Regulation (EU) 2017\/745 \u2013 Introduction to the Regulation<\/a><\/td><td class=\"column-2\">European Regulations - RL12<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\">15\/03 - IP. Orsay<\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-14 even\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl13-regulation-eu-2017-746-on-in-vitro-diagnostic-medical-devices-introduction-to-the-regulation\/\">Regulation (EU) 2017\/746 on In Vitro Diagnostic Medical Devices \u2013 Introduction to the Regulation<\/a><\/td><td class=\"column-2\">European Regulations - RL13<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\">21\/03 - IP. Toulouse ou Virt.<\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-15 odd\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl14-preparation-of-the-technical-documentation-in-accordance-with-regulation-eu-2017-745\/\">Preparation of the Technical Documentation in accordance with Regulation (EU) 2017\/745<\/a><\/td><td class=\"column-2\">European Regulations - RL14<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-16 even\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl15-preparation-of-technical-documentation-in-accordance-with-regulation-eu-2017-746\/\">Preparation of Technical Documentation in accordance with Regulation (EU) 2017\/746<\/a><\/td><td class=\"column-2\">European Regulations - RL15<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-17 odd\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl20-post-market-surveillance-of-medical-devices\/\">Post-Market Surveillance of Medical Devices<\/a><\/td><td class=\"column-2\">European Regulations - RL20<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-18 even\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl21-post-market-surveillance-of-in-vitro-diagnostic-medical-devices\/\">Post-Market Surveillance of In Vitro Diagnostic Medical Devices<\/a><\/td><td class=\"column-2\">European Regulations - RL21<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-19 odd\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl22-regulation-eu-2017-745-compliance-with-the-general-safety-and-performance-requirements\/\">Regulation (EU) 2017\/745: Compliance with the General Safety and Performance Requirements<\/a><\/td><td class=\"column-2\">European Regulations - RL22<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-20 even\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl23-regulation-eu-2017-746-compliance-with-the-general-safety-and-performance-requirements\/\">Regulation (EU) 2017\/746: Compliance with the General Safety and Performance Requirements<\/a><\/td><td class=\"column-2\">European Regulations - RL23<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-21 odd\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl24-in-vitro-diagnostic-medical-devices-european-vigilance-requirements\/\">In Vitro Diagnostic Medical Devices: European Vigilance Requirements<\/a><\/td><td class=\"column-2\">European Regulations - RL24<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-22 even\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/st02-medical-devices-ethylene-oxide-sterilization-application-of-en-iso-11135\/\">Medical Devices: Ethylene Oxide Sterilization \u2013 Application of EN ISO 11135<\/a><\/td><td class=\"column-2\">Processes - ST02<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-23 odd\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/st03-medical-devices-ionizing-radiation-sterilization-application-of-en-iso-11137\/\">Medical Devices: Ionizing Radiation Sterilization \u2013 Application of EN ISO 11137<\/a><\/td><td class=\"column-2\">Processes - ST03<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\">05\/07 - IP. Orsay<\/td>\n<\/tr>\n<tr class=\"row-24 even\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/medical-devices-moist-heat-sterilization-application-of-en-iso-17665-1st04\/\">Medical Devices: Moist Heat Sterilization \u2013 Application of EN ISO 17665-1ST04<\/a><\/td><td class=\"column-2\">Processes - ST04<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<tr class=\"row-25 odd\">\n\t<td class=\"column-1\"><a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/medical-devices-dry-heat-sterilization-application-of-en-iso-20857\/\">Medical Devices: Dry Heat Sterilization \u2013 Application of EN ISO 20857<\/a><\/td><td class=\"column-2\">Processes - ST05<\/td><td class=\"column-3\">1 day<br \/>\n7 hours<\/td><td class=\"column-4\">800,00\u20ac<\/td><td class=\"column-5\"><\/td><td class=\"column-6\"><\/td><td class=\"column-7\"><\/td><td class=\"column-8\"><\/td><td class=\"column-9\"><\/td><td class=\"column-10\"><\/td><td class=\"column-11\"><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<!-- #tablepress-formations-q-r from cache -->\n<\/div><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-324ff52 elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"324ff52\" data-element_type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-e9c6e1a\" data-id=\"e9c6e1a\" data-element_type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t\t\t<div class=\"elementor-element elementor-element-ac1db4e elementor-widget elementor-widget-heading\" data-id=\"ac1db4e\" data-element_type=\"widget\" id=\"catalogue\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">All our European Regulations trainings<\/h2>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-bddac9f elementor-grid-4 elementor-posts__hover-none elementor-posts--thumbnail-none elementor-grid-tablet-2 elementor-grid-mobile-1 elementor-widget elementor-widget-posts\" data-id=\"bddac9f\" data-element_type=\"widget\" data-settings=\"{&quot;cards_columns&quot;:&quot;4&quot;,&quot;cards_row_gap&quot;:{&quot;unit&quot;:&quot;px&quot;,&quot;size&quot;:20,&quot;sizes&quot;:[]},&quot;cards_columns_tablet&quot;:&quot;2&quot;,&quot;cards_columns_mobile&quot;:&quot;1&quot;,&quot;cards_row_gap_tablet&quot;:{&quot;unit&quot;:&quot;px&quot;,&quot;size&quot;:&quot;&quot;,&quot;sizes&quot;:[]},&quot;cards_row_gap_mobile&quot;:{&quot;unit&quot;:&quot;px&quot;,&quot;size&quot;:&quot;&quot;,&quot;sizes&quot;:[]}}\" data-widget_type=\"posts.cards\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<link rel=\"stylesheet\" href=\"https:\/\/ceiso.fr\/en\/wp-content\/plugins\/elementor-pro\/assets\/css\/widget-posts.min.css\">\t\t<div class=\"elementor-posts-container elementor-posts elementor-posts--skin-cards elementor-grid\">\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-519 post type-post status-publish format-standard hentry category-european-regulations category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl12-medical-device-regulation-eu-2017-745-introduction-to-the-regulation\/\" >\n\t\t\t\tRL12 &#8211; Medical Device Regulation (EU) 2017\/745 &#8211; Introduction to the Regulation\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. RL12 &#8211; INTRA \/ INTER EUROPEAN REGULATIONS COURSE DESCRIPTION The design, production and marketing of Medical Devices in Europe<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl12-medical-device-regulation-eu-2017-745-introduction-to-the-regulation\/\" aria-label=\"Read more about RL12 &#8211; Medical Device Regulation (EU) 2017\/745 &#8211; Introduction to the Regulation\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-521 post type-post status-publish format-standard hentry category-european-regulations category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl13-regulation-eu-2017-746-on-in-vitro-diagnostic-medical-devices-introduction-to-the-regulation\/\" >\n\t\t\t\tRL13 &#8211; Regulation (EU) 2017\/746 on In Vitro Diagnostic Medical Devices &#8211; Introduction to the Regulation\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. RL13 &#8211; INTRA \/ INTER EUROPEAN REGULATIONS COURSE DESCRIPTION The design, production and marketing of In Vitro Diagnostic Medical<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl13-regulation-eu-2017-746-on-in-vitro-diagnostic-medical-devices-introduction-to-the-regulation\/\" aria-label=\"Read more about RL13 &#8211; Regulation (EU) 2017\/746 on In Vitro Diagnostic Medical Devices &#8211; Introduction to the Regulation\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-524 post type-post status-publish format-standard hentry category-european-regulations category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl14-preparation-of-the-technical-documentation-in-accordance-with-regulation-eu-2017-745\/\" >\n\t\t\t\tRL14 &#8211; Preparation of the Technical Documentation in accordance with Regulation (EU) 2017\/745\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. RL14 &#8211; INTRA \/ INTER EUROPEAN REGULATIONS COURSE DESCRIPTION To place Medical Devices on the market in Europe, the<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl14-preparation-of-the-technical-documentation-in-accordance-with-regulation-eu-2017-745\/\" aria-label=\"Read more about RL14 &#8211; Preparation of the Technical Documentation in accordance with Regulation (EU) 2017\/745\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-528 post type-post status-publish format-standard hentry category-european-regulations category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl15-preparation-of-technical-documentation-in-accordance-with-regulation-eu-2017-746\/\" >\n\t\t\t\tRL15 &#8211; Preparation of Technical Documentation in accordance with Regulation (EU) 2017\/746\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. RL15 &#8211; INTRA \/ INTER EUROPEAN REGULATIONS COURSE DESCRIPTION To place In Vitro Diagnostic Medical Devices on the market<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl15-preparation-of-technical-documentation-in-accordance-with-regulation-eu-2017-746\/\" aria-label=\"Read more about RL15 &#8211; Preparation of Technical Documentation in accordance with Regulation (EU) 2017\/746\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-531 post type-post status-publish format-standard hentry category-european-regulations category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl07-medical-devicesrl15-european-materiovigilance-requirements\/\" >\n\t\t\t\tRL07 &#8211; Medical Devices: European Materiovigilance Requirements\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. RL07 &#8211; INTRA \/ INTER EUROPEAN REGULATIONS COURSE DESCRIPTION When Medical Devices (MD) are placed on the market in<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl07-medical-devicesrl15-european-materiovigilance-requirements\/\" aria-label=\"Read more about RL07 &#8211; Medical Devices: European Materiovigilance Requirements\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-534 post type-post status-publish format-standard hentry category-european-regulations category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl20-post-market-surveillance-of-medical-devices\/\" >\n\t\t\t\tRL20 &#8211; Post-Market Surveillance of Medical Devices\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. RL20 &#8211; INTRA \/ INTER EUROPEAN REGULATIONS COURSE DESCRIPTION The demonstration of a Medical Device\u2019s compliance with essential requirements<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl20-post-market-surveillance-of-medical-devices\/\" aria-label=\"Read more about RL20 &#8211; Post-Market Surveillance of Medical Devices\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-537 post type-post status-publish format-standard hentry category-european-regulations category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl21-post-market-surveillance-of-in-vitro-diagnostic-medical-devices\/\" >\n\t\t\t\tRL21 &#8211; Post-Market Surveillance of In Vitro Diagnostic Medical Devices\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. RL21 &#8211; INTRA \/ INTER EUROPEAN REGULATIONS COURSE DESCRIPTION The demonstration of an In Vitro Diagnostic Medical Device\u2019s compliance<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl21-post-market-surveillance-of-in-vitro-diagnostic-medical-devices\/\" aria-label=\"Read more about RL21 &#8211; Post-Market Surveillance of In Vitro Diagnostic Medical Devices\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-540 post type-post status-publish format-standard hentry category-european-regulations category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl22-regulation-eu-2017-745-compliance-with-the-general-safety-and-performance-requirements\/\" >\n\t\t\t\tRL22 &#8211; Regulation (EU) 2017\/745: Compliance with the General Safety and Performance Requirements\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. RL22 &#8211; INTRA \/ INTER EUROPEAN REGULATIONS COURSE DESCRIPTION To place Medical Devices on the market in Europe, the<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl22-regulation-eu-2017-745-compliance-with-the-general-safety-and-performance-requirements\/\" aria-label=\"Read more about RL22 &#8211; Regulation (EU) 2017\/745: Compliance with the General Safety and Performance Requirements\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-543 post type-post status-publish format-standard hentry category-european-regulations category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl23-regulation-eu-2017-746-compliance-with-the-general-safety-and-performance-requirements\/\" >\n\t\t\t\tRL23 &#8211; Regulation (EU) 2017\/746: Compliance with the General Safety and Performance Requirements\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. RL23 &#8211; INTRA \/ INTER EUROPEAN REGULATIONS COURSE DESCRIPTION To place In Vitro Diagnostic Medical Devices (IVDMD) on the<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl23-regulation-eu-2017-746-compliance-with-the-general-safety-and-performance-requirements\/\" aria-label=\"Read more about RL23 &#8211; Regulation (EU) 2017\/746: Compliance with the General Safety and Performance Requirements\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-545 post type-post status-publish format-standard hentry category-european-regulations category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl24-in-vitro-diagnostic-medical-devices-european-vigilance-requirements\/\" >\n\t\t\t\tRL24 &#8211; In Vitro Diagnostic Medical Devices: European Vigilance Requirements\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. RL24 &#8211; INTRA \/ INTER EUROPEAN REGULATIONS COURSE DESCRIPTION When in vitro diagnostic medical devices (IVDMD) are placed on<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl24-in-vitro-diagnostic-medical-devices-european-vigilance-requirements\/\" aria-label=\"Read more about RL24 &#8211; In Vitro Diagnostic Medical Devices: European Vigilance Requirements\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<\/div>\n\t\t\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-bb00a75 elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"bb00a75\" data-element_type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-ed00c35\" data-id=\"ed00c35\" data-element_type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t\t\t<div class=\"elementor-element elementor-element-cdf61b3 elementor-widget elementor-widget-heading\" data-id=\"cdf61b3\" data-element_type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">All our International Regulations trainings<\/h2>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-2629440 elementor-grid-4 elementor-posts__hover-none elementor-posts--thumbnail-none elementor-grid-tablet-2 elementor-grid-mobile-1 elementor-widget elementor-widget-posts\" data-id=\"2629440\" data-element_type=\"widget\" data-settings=\"{&quot;cards_columns&quot;:&quot;4&quot;,&quot;cards_row_gap&quot;:{&quot;unit&quot;:&quot;px&quot;,&quot;size&quot;:20,&quot;sizes&quot;:[]},&quot;cards_columns_tablet&quot;:&quot;2&quot;,&quot;cards_columns_mobile&quot;:&quot;1&quot;,&quot;cards_row_gap_tablet&quot;:{&quot;unit&quot;:&quot;px&quot;,&quot;size&quot;:&quot;&quot;,&quot;sizes&quot;:[]},&quot;cards_row_gap_mobile&quot;:{&quot;unit&quot;:&quot;px&quot;,&quot;size&quot;:&quot;&quot;,&quot;sizes&quot;:[]}}\" data-widget_type=\"posts.cards\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<div class=\"elementor-posts-container elementor-posts elementor-posts--skin-cards elementor-grid\">\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-510 post type-post status-publish format-standard hentry category-international-regulations category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl08-compliance-with-us-market-authorization-requirements-for-medical-devices-510k-submission\/\" >\n\t\t\t\tRL08 &#8211; Compliance with US Market Authorization Requirements for Medical Devices &#8211; 510(k) Submission\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. RL08 &#8211; INTRA \/ INTER INTERNATIONAL REGULATIONS COURSE DESCRIPTION Compliance with FDA (Food and Drug Administration) requirements is mandatory<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/rl08-compliance-with-us-market-authorization-requirements-for-medical-devices-510k-submission\/\" aria-label=\"Read more about RL08 &#8211; Compliance with US Market Authorization Requirements for Medical Devices &#8211; 510(k) Submission\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<\/div>\n\t\t\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-fbf7150 elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"fbf7150\" data-element_type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-4e4b274\" data-id=\"4e4b274\" data-element_type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t\t\t<div class=\"elementor-element elementor-element-a19cda2 elementor-widget elementor-widget-heading\" data-id=\"a19cda2\" data-element_type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">All our Quality System trainings<\/h2>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-744ea83 elementor-grid-4 elementor-posts__hover-none elementor-posts--thumbnail-none elementor-grid-tablet-2 elementor-grid-mobile-1 elementor-widget elementor-widget-posts\" data-id=\"744ea83\" data-element_type=\"widget\" data-settings=\"{&quot;cards_columns&quot;:&quot;4&quot;,&quot;cards_row_gap&quot;:{&quot;unit&quot;:&quot;px&quot;,&quot;size&quot;:20,&quot;sizes&quot;:[]},&quot;cards_columns_tablet&quot;:&quot;2&quot;,&quot;cards_columns_mobile&quot;:&quot;1&quot;,&quot;cards_row_gap_tablet&quot;:{&quot;unit&quot;:&quot;px&quot;,&quot;size&quot;:&quot;&quot;,&quot;sizes&quot;:[]},&quot;cards_row_gap_mobile&quot;:{&quot;unit&quot;:&quot;px&quot;,&quot;size&quot;:&quot;&quot;,&quot;sizes&quot;:[]}}\" data-widget_type=\"posts.cards\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<div class=\"elementor-posts-container elementor-posts elementor-posts--skin-cards elementor-grid\">\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-487 post type-post status-publish format-standard hentry category-quality-system category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq03-quality-management-system-for-medical-devices\/\" >\n\t\t\t\tMQ03 &#8211; Quality Management System for Medical Devices\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. MQ03 &#8211; INTRA \/ INTER QUALITY SYSTEM COURSE DESCRIPTION CE-marking requires the implementation of a Quality organization. European standard<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq03-quality-management-system-for-medical-devices\/\" aria-label=\"Read more about MQ03 &#8211; Quality Management System for Medical Devices\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-490 post type-post status-publish format-standard hentry category-quality-system category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq05-quality-audits-according-to-iso-19011\/\" >\n\t\t\t\tMQ05 &#8211; Quality Audits according to ISO 19011\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. MQ05 &#8211; INTRA \/ INTER QUALITY SYSTEM COURSE DESCRIPTION This course will allow you to acquire practical knowledge to<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq05-quality-audits-according-to-iso-19011\/\" aria-label=\"Read more about MQ05 &#8211; Quality Audits according to ISO 19011\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-497 post type-post status-publish format-standard hentry category-quality-system category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq06-validation-of-processes-applied-to-medical-devices-and-in-vitro-diagnostic-medical-devices\/\" >\n\t\t\t\tMQ06 &#8211; Validation of Processes applied to Medical Devices and In Vitro Diagnostic Medical Devices\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. MQ06 &#8211; INTRA \/ INTER QUALITY SYSTEM COURSE DESCRIPTION Applicable regulations require control of the production of medical devices<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq06-validation-of-processes-applied-to-medical-devices-and-in-vitro-diagnostic-medical-devices\/\" aria-label=\"Read more about MQ06 &#8211; Validation of Processes applied to Medical Devices and In Vitro Diagnostic Medical Devices\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-499 post type-post status-publish format-standard hentry category-quality-system category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq10-validation-of-software-applications\/\" >\n\t\t\t\tMQ10 &#8211; Validation of Software Applications\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. MQ10 &#8211; INTRA \/ INTER QUALITY SYSTEM COURSE DESCRIPTION This course will allow you to acquire practical knowledge to<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq10-validation-of-software-applications\/\" aria-label=\"Read more about MQ10 &#8211; Validation of Software Applications\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<\/div>\n\t\t\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-ddb6878 elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"ddb6878\" data-element_type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-53b01a0\" data-id=\"53b01a0\" data-element_type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t\t\t<div class=\"elementor-element elementor-element-e2bbced elementor-widget elementor-widget-heading\" data-id=\"e2bbced\" data-element_type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">All our Processes trainings<\/h2>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-f0fb503 elementor-grid-4 elementor-posts__hover-none elementor-posts--thumbnail-none elementor-grid-tablet-2 elementor-grid-mobile-1 elementor-widget elementor-widget-posts\" data-id=\"f0fb503\" data-element_type=\"widget\" data-settings=\"{&quot;cards_columns&quot;:&quot;4&quot;,&quot;cards_row_gap&quot;:{&quot;unit&quot;:&quot;px&quot;,&quot;size&quot;:20,&quot;sizes&quot;:[]},&quot;cards_columns_tablet&quot;:&quot;2&quot;,&quot;cards_columns_mobile&quot;:&quot;1&quot;,&quot;cards_row_gap_tablet&quot;:{&quot;unit&quot;:&quot;px&quot;,&quot;size&quot;:&quot;&quot;,&quot;sizes&quot;:[]},&quot;cards_row_gap_mobile&quot;:{&quot;unit&quot;:&quot;px&quot;,&quot;size&quot;:&quot;&quot;,&quot;sizes&quot;:[]}}\" data-widget_type=\"posts.cards\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<div class=\"elementor-posts-container elementor-posts elementor-posts--skin-cards elementor-grid\">\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-487 post type-post status-publish format-standard hentry category-quality-system category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq03-quality-management-system-for-medical-devices\/\" >\n\t\t\t\tMQ03 &#8211; Quality Management System for Medical Devices\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. MQ03 &#8211; INTRA \/ INTER QUALITY SYSTEM COURSE DESCRIPTION CE-marking requires the implementation of a Quality organization. European standard<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq03-quality-management-system-for-medical-devices\/\" aria-label=\"Read more about MQ03 &#8211; Quality Management System for Medical Devices\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-490 post type-post status-publish format-standard hentry category-quality-system category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq05-quality-audits-according-to-iso-19011\/\" >\n\t\t\t\tMQ05 &#8211; Quality Audits according to ISO 19011\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. MQ05 &#8211; INTRA \/ INTER QUALITY SYSTEM COURSE DESCRIPTION This course will allow you to acquire practical knowledge to<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq05-quality-audits-according-to-iso-19011\/\" aria-label=\"Read more about MQ05 &#8211; Quality Audits according to ISO 19011\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-497 post type-post status-publish format-standard hentry category-quality-system category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq06-validation-of-processes-applied-to-medical-devices-and-in-vitro-diagnostic-medical-devices\/\" >\n\t\t\t\tMQ06 &#8211; Validation of Processes applied to Medical Devices and In Vitro Diagnostic Medical Devices\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. MQ06 &#8211; INTRA \/ INTER QUALITY SYSTEM COURSE DESCRIPTION Applicable regulations require control of the production of medical devices<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq06-validation-of-processes-applied-to-medical-devices-and-in-vitro-diagnostic-medical-devices\/\" aria-label=\"Read more about MQ06 &#8211; Validation of Processes applied to Medical Devices and In Vitro Diagnostic Medical Devices\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-499 post type-post status-publish format-standard hentry category-quality-system category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq10-validation-of-software-applications\/\" >\n\t\t\t\tMQ10 &#8211; Validation of Software Applications\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. MQ10 &#8211; INTRA \/ INTER QUALITY SYSTEM COURSE DESCRIPTION This course will allow you to acquire practical knowledge to<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/mq10-validation-of-software-applications\/\" aria-label=\"Read more about MQ10 &#8211; Validation of Software Applications\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<\/div>\n\t\t\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-9e3a465 elementor-grid-4 elementor-posts__hover-none elementor-posts--thumbnail-none elementor-grid-tablet-2 elementor-grid-mobile-1 elementor-widget elementor-widget-posts\" data-id=\"9e3a465\" data-element_type=\"widget\" data-settings=\"{&quot;cards_columns&quot;:&quot;4&quot;,&quot;cards_row_gap&quot;:{&quot;unit&quot;:&quot;px&quot;,&quot;size&quot;:20,&quot;sizes&quot;:[]},&quot;cards_columns_tablet&quot;:&quot;2&quot;,&quot;cards_columns_mobile&quot;:&quot;1&quot;,&quot;cards_row_gap_tablet&quot;:{&quot;unit&quot;:&quot;px&quot;,&quot;size&quot;:&quot;&quot;,&quot;sizes&quot;:[]},&quot;cards_row_gap_mobile&quot;:{&quot;unit&quot;:&quot;px&quot;,&quot;size&quot;:&quot;&quot;,&quot;sizes&quot;:[]}}\" data-widget_type=\"posts.cards\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<div class=\"elementor-posts-container elementor-posts elementor-posts--skin-cards elementor-grid\">\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-558 post type-post status-publish format-standard hentry category-processes category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/st02-medical-devices-ethylene-oxide-sterilization-application-of-en-iso-11135\/\" >\n\t\t\t\tST02 &#8211; Medical Devices: Ethylene Oxide Sterilization &#8211; Application of EN ISO 11135\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. ST02 &#8211; INTRA \/ INTER PROCESSES COURSE DESCRIPTION International regulations that govern market authorizations for Medical Devices require process<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/st02-medical-devices-ethylene-oxide-sterilization-application-of-en-iso-11135\/\" aria-label=\"Read more about ST02 &#8211; Medical Devices: Ethylene Oxide Sterilization &#8211; Application of EN ISO 11135\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-561 post type-post status-publish format-standard hentry category-processes category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/st03-medical-devices-ionizing-radiation-sterilization-application-of-en-iso-11137\/\" >\n\t\t\t\tST03 &#8211; Medical Devices: Ionizing Radiation Sterilization &#8211; Application of EN ISO 11137\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. ST03 &#8211; INTRA \/ INTER PROCESSES COURSE DESCRIPTION International regulations that govern market authorization for Medical Devices require process<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/st03-medical-devices-ionizing-radiation-sterilization-application-of-en-iso-11137\/\" aria-label=\"Read more about ST03 &#8211; Medical Devices: Ionizing Radiation Sterilization &#8211; Application of EN ISO 11137\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-563 post type-post status-publish format-standard hentry category-processes category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/medical-devices-moist-heat-sterilization-application-of-en-iso-17665-1st04\/\" >\n\t\t\t\tST04 &#8211; Medical Devices: Moist Heat Sterilization &#8211; Application of EN ISO 17665-1ST04\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. ST04 &#8211; INTRA \/ INTER PROCESSES COURSE DESCRIPTION International regulations that govern market authorization for Medical Devices require process<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/medical-devices-moist-heat-sterilization-application-of-en-iso-17665-1st04\/\" aria-label=\"Read more about ST04 &#8211; Medical Devices: Moist Heat Sterilization &#8211; Application of EN ISO 17665-1ST04\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-567 post type-post status-publish format-standard hentry category-processes category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/medical-devices-dry-heat-sterilization-application-of-en-iso-20857\/\" >\n\t\t\t\tST05 &#8211; Medical Devices: Dry Heat Sterilization &#8211; Application of EN ISO 20857\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. ST05 &#8211; INTRA \/ INTER PROCESSES COURSE DESCRIPTION International regulations that govern market authorization for Medical Devices require process<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/medical-devices-dry-heat-sterilization-application-of-en-iso-20857\/\" aria-label=\"Read more about ST05 &#8211; Medical Devices: Dry Heat Sterilization &#8211; Application of EN ISO 20857\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<\/div>\n\t\t\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-09a114d elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"09a114d\" data-element_type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-2e6c750\" data-id=\"2e6c750\" data-element_type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t\t\t<div class=\"elementor-element elementor-element-d9ae05f elementor-widget elementor-widget-heading\" data-id=\"d9ae05f\" data-element_type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">All our Risks trainings<\/h2>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-de945e5 elementor-grid-4 elementor-posts__hover-none elementor-posts--thumbnail-none elementor-grid-tablet-2 elementor-grid-mobile-1 elementor-widget elementor-widget-posts\" data-id=\"de945e5\" data-element_type=\"widget\" data-settings=\"{&quot;cards_columns&quot;:&quot;4&quot;,&quot;cards_row_gap&quot;:{&quot;unit&quot;:&quot;px&quot;,&quot;size&quot;:20,&quot;sizes&quot;:[]},&quot;cards_columns_tablet&quot;:&quot;2&quot;,&quot;cards_columns_mobile&quot;:&quot;1&quot;,&quot;cards_row_gap_tablet&quot;:{&quot;unit&quot;:&quot;px&quot;,&quot;size&quot;:&quot;&quot;,&quot;sizes&quot;:[]},&quot;cards_row_gap_mobile&quot;:{&quot;unit&quot;:&quot;px&quot;,&quot;size&quot;:&quot;&quot;,&quot;sizes&quot;:[]}}\" data-widget_type=\"posts.cards\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<div class=\"elementor-posts-container elementor-posts elementor-posts--skin-cards elementor-grid\">\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-463 post type-post status-publish format-standard hentry category-managing-risks category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/gr02-medical-devices-risk-management\/\" >\n\t\t\t\tGR02 &#8211; Medical Devices: Risk Management\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. GR02 &#8211; INTRA \/ INTER MANAGING RISKS COURSE DESCRIPTION This training will allow you to update or acquire practical<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/gr02-medical-devices-risk-management\/\" aria-label=\"Read more about GR02 &#8211; Medical Devices: Risk Management\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-466 post type-post status-publish format-standard hentry category-managing-risks category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/gr03-medical-device-software-development\/\" >\n\t\t\t\tGR03 &#8211; Medical Device Software Development\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. GR03 &#8211; INTRA \/ INTER MANAGING RISKS COURSE DESCRIPTION At the end of this course, participants will understand the<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/gr03-medical-device-software-development\/\" aria-label=\"Read more about GR03 &#8211; Medical Device Software Development\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-469 post type-post status-publish format-standard hentry category-managing-risks category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/gr04-safety-and-essential-performance-requirements-for-medical-electrical-equipment-en-60601-1\/\" >\n\t\t\t\tGR04 &#8211; Safety and Essential Performance Requirements for Medical Electrical Equipment &#8211; EN 60601-1\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. GR04 &#8211; INTRA \/ INTER MANAGING RISKS COURSE DESCRIPTION To place Medical Devices (MD) on the market in Europe,<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/gr04-safety-and-essential-performance-requirements-for-medical-electrical-equipment-en-60601-1\/\" aria-label=\"Read more about GR04 &#8211; Safety and Essential Performance Requirements for Medical Electrical Equipment &#8211; EN 60601-1\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-472 post type-post status-publish format-standard hentry category-managing-risks category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/gr05-application-of-usability-engineering\/\" >\n\t\t\t\tGR05 &#8211; Application of Usability Engineering\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. GR05 &#8211; INTRA \/ INTER MANAGING RISKS COURSE DESCRIPTION At the end of the course, participants will better understand<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/gr05-application-of-usability-engineering\/\" aria-label=\"Read more about GR05 &#8211; Application of Usability Engineering\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<article class=\"elementor-post elementor-grid-item post-474 post type-post status-publish format-standard hentry category-managing-risks category-regulatory-quality-trainings\">\n\t\t\t<div class=\"elementor-post__card\">\n\t\t\t\t<div class=\"elementor-post__text\">\n\t\t\t\t<h3 class=\"elementor-post__title\">\n\t\t\t<a href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/gr06-biological-evaluation-of-medical-devices-according-to-en-iso-10993-1\/\" >\n\t\t\t\tGR06 &#8211; Biological Evaluation of Medical Devices according to EN ISO 10993-1\t\t\t<\/a>\n\t\t<\/h3>\n\t\t\t\t<div class=\"elementor-post__excerpt\">\n\t\t\t<p>REF. GR06 &#8211; INTRA \/ INTER MANAGING RISKS COURSE DESCRIPTION To place Medical Devices on the market in Europe, the<\/p>\n\t\t<\/div>\n\t\t\n\t\t<a class=\"elementor-post__read-more\" href=\"https:\/\/ceiso.fr\/en\/regulatory-quality-trainings\/gr06-biological-evaluation-of-medical-devices-according-to-en-iso-10993-1\/\" aria-label=\"Read more about GR06 &#8211; Biological Evaluation of Medical Devices according to EN ISO 10993-1\" >\n\t\t\tSee the training &gt;\t\t<\/a>\n\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/article>\n\t\t\t\t<\/div>\n\t\t\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-7d43dae elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"7d43dae\" data-element_type=\"section\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-50 elementor-top-column elementor-element elementor-element-b7fd431\" data-id=\"b7fd431\" data-element_type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t\t\t<div class=\"elementor-element elementor-element-c45d661 elementor-widget elementor-widget-heading\" data-id=\"c45d661\" data-element_type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">Questions? Book a training course? Contact us!<\/h2>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-66193e2 elementor-widget elementor-widget-text-editor\" data-id=\"66193e2\" data-element_type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<p>Does your problem concern the Quality System, Risk Management, Processes or Regulations? Please specify your need via the contact form.<\/p><p>We will get back to you as soon as possible.<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t<div class=\"elementor-column elementor-col-50 elementor-top-column elementor-element elementor-element-4b8415d\" data-id=\"4b8415d\" data-element_type=\"column\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t\t\t<div class=\"elementor-element elementor-element-7b8108a elementor-button-align-start elementor-widget elementor-widget-form\" data-id=\"7b8108a\" data-element_type=\"widget\" data-settings=\"{&quot;step_next_label&quot;:&quot;Next&quot;,&quot;step_previous_label&quot;:&quot;Previous&quot;,&quot;button_width&quot;:&quot;100&quot;,&quot;step_type&quot;:&quot;number_text&quot;,&quot;step_icon_shape&quot;:&quot;circle&quot;}\" data-widget_type=\"form.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<style>\/*! elementor-pro - v3.12.2 - 09-04-2023 *\/\n.elementor-button.elementor-hidden,.elementor-hidden{display:none}.e-form__step{width:100%}.e-form__step:not(.elementor-hidden){display:flex;flex-wrap:wrap}.e-form__buttons{flex-wrap:wrap}.e-form__buttons,.e-form__buttons__wrapper{display:flex}.e-form__indicators{display:flex;justify-content:space-between;align-items:center;flex-wrap:nowrap;font-size:13px;margin-bottom:var(--e-form-steps-indicators-spacing)}.e-form__indicators__indicator{display:flex;flex-direction:column;align-items:center;justify-content:center;flex-basis:0;padding:0 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elementor-mark-required\">\n\t\t\t\t\t\t\t\t\t\t\t\t<label for=\"form-field-nom\" class=\"elementor-field-label\">\n\t\t\t\t\t\t\t\tLast name\t\t\t\t\t\t\t<\/label>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<input size=\"1\" type=\"text\" name=\"form_fields[nom]\" id=\"form-field-nom\" class=\"elementor-field elementor-size-sm  elementor-field-textual\" placeholder=\"Last name\" required=\"required\" aria-required=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<div class=\"elementor-field-type-text elementor-field-group elementor-column elementor-field-group-prenom elementor-col-50 elementor-field-required elementor-mark-required\">\n\t\t\t\t\t\t\t\t\t\t\t\t<label for=\"form-field-prenom\" class=\"elementor-field-label\">\n\t\t\t\t\t\t\t\tFirst name\t\t\t\t\t\t\t<\/label>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<input size=\"1\" type=\"text\" name=\"form_fields[prenom]\" id=\"form-field-prenom\" class=\"elementor-field elementor-size-sm  elementor-field-textual\" placeholder=\"First name\" required=\"required\" aria-required=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<div class=\"elementor-field-type-email elementor-field-group elementor-column elementor-field-group-email elementor-col-100 elementor-field-required elementor-mark-required\">\n\t\t\t\t\t\t\t\t\t\t\t\t<label for=\"form-field-email\" class=\"elementor-field-label\">\n\t\t\t\t\t\t\t\tEmail address\t\t\t\t\t\t\t<\/label>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<input size=\"1\" type=\"email\" name=\"form_fields[email]\" id=\"form-field-email\" class=\"elementor-field elementor-size-sm  elementor-field-textual\" placeholder=\"first.last@company.com\" required=\"required\" aria-required=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<div class=\"elementor-field-type-text elementor-field-group elementor-column elementor-field-group-societe elementor-col-100 elementor-field-required elementor-mark-required\">\n\t\t\t\t\t\t\t\t\t\t\t\t<label for=\"form-field-societe\" class=\"elementor-field-label\">\n\t\t\t\t\t\t\t\tCompany\t\t\t\t\t\t\t<\/label>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<input size=\"1\" type=\"text\" name=\"form_fields[societe]\" id=\"form-field-societe\" class=\"elementor-field elementor-size-sm  elementor-field-textual\" placeholder=\"Company\" required=\"required\" aria-required=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<div class=\"elementor-field-type-text elementor-field-group elementor-column elementor-field-group-field_2cc6d30 elementor-col-100 elementor-field-required elementor-mark-required\">\n\t\t\t\t\t\t\t\t\t\t\t\t<label for=\"form-field-field_2cc6d30\" class=\"elementor-field-label\">\n\t\t\t\t\t\t\t\tPosition\t\t\t\t\t\t\t<\/label>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<input size=\"1\" type=\"text\" name=\"form_fields[field_2cc6d30]\" id=\"form-field-field_2cc6d30\" class=\"elementor-field elementor-size-sm  elementor-field-textual\" placeholder=\"Your position\" required=\"required\" aria-required=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<div class=\"elementor-field-type-tel elementor-field-group elementor-column elementor-field-group-field_7fb3308 elementor-col-100\">\n\t\t\t\t\t\t\t\t\t\t\t\t<label for=\"form-field-field_7fb3308\" class=\"elementor-field-label\">\n\t\t\t\t\t\t\t\tPhone\t\t\t\t\t\t\t<\/label>\n\t\t\t\t\t\t\t\t<input size=\"1\" type=\"tel\" name=\"form_fields[field_7fb3308]\" id=\"form-field-field_7fb3308\" class=\"elementor-field elementor-size-sm  elementor-field-textual\" placeholder=\"Your phone number\" pattern=\"[0-9()#&amp;+*-=.]+\" title=\"Only numbers and phone characters (#, -, *, etc) are accepted.\">\n\n\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<div class=\"elementor-field-type-textarea elementor-field-group elementor-column elementor-field-group-message elementor-col-100\">\n\t\t\t\t\t\t\t\t\t\t\t\t<label for=\"form-field-message\" class=\"elementor-field-label\">\n\t\t\t\t\t\t\t\tYour message\t\t\t\t\t\t\t<\/label>\n\t\t\t\t\t\t<textarea class=\"elementor-field-textual elementor-field  elementor-size-sm\" name=\"form_fields[message]\" id=\"form-field-message\" rows=\"4\" placeholder=\"Type your message here...\"><\/textarea>\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<div class=\"elementor-field-type-recaptcha_v3 elementor-field-group elementor-column elementor-field-group-recaptcha elementor-col-100 recaptcha_v3-bottomright\">\n\t\t\t\t\t<div class=\"elementor-field\" id=\"form-field-recaptcha\"><div class=\"elementor-g-recaptcha\" data-sitekey=\"6Ld02rglAAAAACQxMQIdi63gdEsFjk7X1BY5tD8l\" data-type=\"v3\" data-action=\"Form\" data-badge=\"bottomright\" data-size=\"invisible\"><\/div><\/div>\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<div class=\"elementor-field-group elementor-column elementor-field-type-submit elementor-col-100 e-form__buttons\">\n\t\t\t\t\t<button type=\"submit\" class=\"elementor-button elementor-size-sm\">\n\t\t\t\t\t\t<span >\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\" elementor-button-icon\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-button-text\">Send<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t<\/button>\n\t\t\t\t<\/div>\n\t\t\t<\/div>\n\t\t<\/form>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>Discover our Quality-Regulatory training catalog You work in a demanding regulatory and normative environment. Your employees\u2019 efficiency is an essential part of your company&#8217;s performance. We support the development and maintenance of your teams\u2019 skills. See the catalog See the schedule Information and training schedule All our trainings courses can be carried out either INTER [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":[],"_links":{"self":[{"href":"https:\/\/ceiso.fr\/en\/wp-json\/wp\/v2\/pages\/162"}],"collection":[{"href":"https:\/\/ceiso.fr\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/ceiso.fr\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/ceiso.fr\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/ceiso.fr\/en\/wp-json\/wp\/v2\/comments?post=162"}],"version-history":[{"count":49,"href":"https:\/\/ceiso.fr\/en\/wp-json\/wp\/v2\/pages\/162\/revisions"}],"predecessor-version":[{"id":1172,"href":"https:\/\/ceiso.fr\/en\/wp-json\/wp\/v2\/pages\/162\/revisions\/1172"}],"wp:attachment":[{"href":"https:\/\/ceiso.fr\/en\/wp-json\/wp\/v2\/media?parent=162"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}