{"id":674,"date":"2019-01-07T01:58:21","date_gmt":"2019-01-07T01:58:21","guid":{"rendered":"https:\/\/staging.vantagebiotrials.com\/?p=674"},"modified":"2024-03-17T23:00:44","modified_gmt":"2024-03-17T23:00:44","slug":"vantage-biotrials-passes-health-canada-inspection","status":"publish","type":"post","link":"https:\/\/vantagebiotrials.com\/fr\/vantage-biotrials-passes-health-canada-inspection\/","title":{"rendered":"Vantage BioTrials Passes Health Canada Inspection"},"content":{"rendered":"<p><strong>January 7, 2019, Montreal, Canada <\/strong>&#8211; Earlier this year, Vantage BioTrials (VBT) took a very important step forward by volunteering to take part in the first of its kind Health Canada pilot inspection program. The program focused on VBT&#8217;s internal processes, procedures &amp; protocol specific studies.<\/p>\n<blockquote>\n<h3 style=\"text-align: center;\"><em>&#8220;Through our dedication &amp; transparency for adhering to quality principles, we continue to add tangible credibility towards achieving operational excellence for our clients, patient groups &amp; partners&#8221;<\/em><\/h3>\n<p style=\"text-align: right;\">Vatche Bartekian, President<\/p>\n<\/blockquote>\n<p>Vantage BioTrials was one of two Clinical Trial Management CRO&#8217;s chosen by Health Canada in 2018. &#8220;Even though their pilot inspection program will be extended into 2019, it is a major accomplishment for us (VBT) to have set a marker for other companies to follow. Through our compliance, we demonstrated\u00a0that our processes, procedures, Corrective Action\/Preventive Action (<strong>CAPA<\/strong>), <strong>Risk-based Monitoring<\/strong> &amp; <strong>Risk-based Trial Management <\/strong>approaches are sound.&#8221; adds Vahe Bartekian, Vice-President of Quality Management.<\/p>\n<p>Vantage BioTrials looks forward to the years ahead by continuing to add value to the Phase I-IV &amp; medical device clinical development needs of its clients, patient groups &amp; partners.<\/p>\n<h3><strong>About us<\/strong><\/h3>\n<p>Founded in 2007, Vantage BioTrials is a privately-held Contract Research Organization (CRO) that provides Phase I-IV clinical trial management services and implements Risk-Based Management through the use of Quality by Design (QbD) methodologies, all delivered to international pharmaceutical, biotechnology, generic pharmaceutical and medical device companies.<\/p>\n<p>Follow us on\u00a0<a href=\"https:\/\/ca.linkedin.com\/company\/vantage-biotrials-inc-\" target=\"_blank\" rel=\"noopener\">LinkedIn<\/a>\u00a0and\u00a0<a href=\"https:\/\/twitter.com\/vantagebt\" target=\"_blank\" rel=\"noopener\">Twitter<\/a>.<\/p>","protected":false},"excerpt":{"rendered":"<p>January 7, 2019, Montreal, Canada &#8211; Earlier this year, Vantage BioTrials (VBT) took a very important step forward by volunteering to take part in the first of its kind Health Canada pilot inspection program. The program focused on VBT&#8217;s internal processes, procedures &amp; protocol specific studies. &#8220;Through our dedication &amp; transparency for adhering to quality principles, we continue to add tangible credibility towards achieving operational excellence for our clients, patient groups &amp; partners&#8221; Vatche Bartekian, President Vantage BioTrials was one of two Clinical Trial Management CRO&#8217;s chosen by Health Canada in 2018. &#8220;Even though their pilot inspection program will be extended into 2019, it is a major accomplishment for us (VBT) to have set a marker for other companies to follow. Through our compliance, we demonstrated\u00a0that our processes, procedures, Corrective Action\/Preventive Action (CAPA), Risk-based Monitoring &amp; Risk-based Trial Management approaches are sound.&#8221; adds Vahe Bartekian, Vice-President of Quality Management. Vantage BioTrials looks forward to the years ahead by continuing to add value to the Phase I-IV &amp; medical device clinical development needs of its clients, patient groups &amp; partners. About us Founded in 2007, Vantage BioTrials is a privately-held Contract Research Organization (CRO) that provides Phase I-IV clinical trial management services and implements Risk-Based Management through the use of Quality by Design (QbD) methodologies, all delivered to international pharmaceutical, biotechnology, generic pharmaceutical and medical device companies. Follow us on\u00a0LinkedIn\u00a0and\u00a0Twitter.<\/p>","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"om_disable_all_campaigns":false,"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"categories":[20],"tags":[],"class_list":["post-674","post","type-post","status-publish","format-standard","hentry","category-news-pressroom","cms-no-post-thumbnail"],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/vantagebiotrials.com\/fr\/wp-json\/wp\/v2\/posts\/674","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/vantagebiotrials.com\/fr\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/vantagebiotrials.com\/fr\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/vantagebiotrials.com\/fr\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/vantagebiotrials.com\/fr\/wp-json\/wp\/v2\/comments?post=674"}],"version-history":[{"count":0,"href":"https:\/\/vantagebiotrials.com\/fr\/wp-json\/wp\/v2\/posts\/674\/revisions"}],"wp:attachment":[{"href":"https:\/\/vantagebiotrials.com\/fr\/wp-json\/wp\/v2\/media?parent=674"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/vantagebiotrials.com\/fr\/wp-json\/wp\/v2\/categories?post=674"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/vantagebiotrials.com\/fr\/wp-json\/wp\/v2\/tags?post=674"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}