{"id":50,"date":"2023-08-22T02:04:49","date_gmt":"2023-08-22T02:04:49","guid":{"rendered":"https:\/\/staging.vantagebiotrials.com\/?page_id=50"},"modified":"2026-05-11T18:52:31","modified_gmt":"2026-05-11T18:52:31","slug":"resources","status":"publish","type":"page","link":"https:\/\/vantagebiotrials.com\/fr\/resources\/","title":{"rendered":"Resources"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-page\" data-elementor-id=\"50\" class=\"elementor elementor-50\">\n\t\t\t\t\t\t<div class=\"elementor-section elementor-top-section elementor-element elementor-element-a579b40 elementor-section-full_width elementor-section-stretched elementor-section-height-default elementor-section-height-default cms-remove-row-no cms-section-no-padding-no cms-full-content-with-space-none cms-boxed-bg-false cms-section-boxed-divider-false cms-overlay-gradient-bg-yes cms-overlay-gradient-mode-tb\" data-id=\"a579b40\" data-element_type=\"section\" data-e-type=\"section\" data-settings=\"{&quot;stretch_section&quot;:&quot;section-stretched&quot;}\">\r\n\t\t\t<div class=\"cms-overlay-gradient\"><\/div><div class=\"cms-section-boxed-bg\"><\/div><div class=\"cms-section-boxed-divider\"><\/div><div class=\"cms-elementor-section-remove\"><\/div><div class=\"cms-elementor-section-corner cms-elementor-section-corner-top\"><\/div><div class=\"cms-elementor-section-corner cms-elementor-section-corner-bottom\"><\/div>\t\t\t<div class=\"elementor-container elementor-column-gap-no \" >\r\n\t\t\t        <div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-92c1d57\" data-id=\"92c1d57\" data-element_type=\"column\" data-e-type=\"column\">\r\n            <div class=\"elementor-widget-wrap elementor-element-populated\">\r\n                \t\t<div class=\"elementor-element elementor-element-aa2f615 elementor-widget elementor-widget-slider_revolution\" data-id=\"aa2f615\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"slider_revolution.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\n\t\t<div class=\"wp-block-themepunch-revslider\">\n\t\t\t<!-- START resources REVOLUTION SLIDER 6.7.18 --><p class=\"rs-p-wp-fix\"><\/p>\n\t\t\t<rs-module-wrap id=\"rev_slider_14_1_wrapper\" data-source=\"gallery\" style=\"visibility:hidden;background:transparent;padding:0;margin:0px auto;margin-top:0;margin-bottom:0;\">\n\t\t\t\t<rs-module id=\"rev_slider_14_1\" style=\"\" data-version=\"6.7.18\">\n\t\t\t\t\t<rs-slides style=\"overflow: hidden; position: absolute;\">\n\t\t\t\t\t\t<rs-slide style=\"position: absolute;\" data-key=\"rs-16\" data-title=\"Slide\" data-in=\"o:1;\" data-out=\"o:1;\">\n\t\t\t\t\t\t\t<img fetchpriority=\"high\" decoding=\"async\" src=\"\/\/vantagebiotrials.com\/wp-content\/plugins\/revslider\/sr6\/assets\/assets\/dummy.png\" alt=\"\" title=\"carabiner.jpg\" width=\"2000\" height=\"1331\" class=\"rev-slidebg tp-rs-img rs-lazyload\" data-lazyload=\"\/\/vantagebiotrials.com\/wp-content\/uploads\/revslider\/resources\/carabiner.jpg\" data-parallax=\"5\" data-no-retina>\n<!--\n\t\t\t\t\t\t\t--><rs-layer\n\t\t\t\t\t\t\t\tid=\"slider-14-slide-16-layer-5\" \n\t\t\t\t\t\t\t\tdata-type=\"image\"\n\t\t\t\t\t\t\t\tdata-rsp_ch=\"on\"\n\t\t\t\t\t\t\t\tdata-xy=\"x:-327px;y:-68px;\"\n\t\t\t\t\t\t\t\tdata-text=\"l:22;\"\n\t\t\t\t\t\t\t\tdata-dim=\"w:1348px;h:633px;\"\n\t\t\t\t\t\t\t\tdata-frame_0=\"tp:600;\"\n\t\t\t\t\t\t\t\tdata-frame_1=\"tp:600;e:power2.inOut;st:1360;\"\n\t\t\t\t\t\t\t\tdata-frame_999=\"o:0;tp:600;e:nothing;st:w;\"\n\t\t\t\t\t\t\t\tstyle=\"z-index:5;\"\n\t\t\t\t\t\t\t><img decoding=\"async\" src=\"\/\/vantagebiotrials.com\/wp-content\/plugins\/revslider\/sr6\/assets\/assets\/dummy.png\" alt=\"\" class=\"tp-rs-img rs-lazyload\" width=\"1348\" height=\"633\" data-lazyload=\"\/\/vantagebiotrials.com\/wp-content\/uploads\/revslider\/slider-ihr-1\/cloud.png\" data-no-retina> \n\t\t\t\t\t\t\t<\/rs-layer><!--\n\n\t\t\t\t\t\t\t--><rs-layer\n\t\t\t\t\t\t\t\tid=\"slider-14-slide-16-layer-2\" \n\t\t\t\t\t\t\t\tdata-type=\"text\"\n\t\t\t\t\t\t\t\tdata-color=\"rgba(51,51,51,1)\"\n\t\t\t\t\t\t\t\tdata-rsp_ch=\"on\"\n\t\t\t\t\t\t\t\tdata-xy=\"x:88px;y:162px;\"\n\t\t\t\t\t\t\t\tdata-text=\"s:40;l:40;fw:700;\"\n\t\t\t\t\t\t\t\tdata-frame_0=\"x:50px;tp:600;\"\n\t\t\t\t\t\t\t\tdata-frame_1=\"tp:600;e:easeOutExpo;st:700;sp:1000;\"\n\t\t\t\t\t\t\t\tdata-frame_999=\"o:0;tp:600;e:nothing;st:w;\"\n\t\t\t\t\t\t\t\tstyle=\"z-index:6;font-family:'Poppins';text-transform:uppercase;\"\n\t\t\t\t\t\t\t>The Business of Trust. \n\t\t\t\t\t\t\t<\/rs-layer><!--\n\n\t\t\t\t\t\t\t--><rs-layer\n\t\t\t\t\t\t\t\tid=\"slider-14-slide-16-layer-3\" \n\t\t\t\t\t\t\t\tdata-type=\"text\"\n\t\t\t\t\t\t\t\tdata-color=\"rgba(51,51,51,1)\"\n\t\t\t\t\t\t\t\tdata-rsp_ch=\"on\"\n\t\t\t\t\t\t\t\tdata-xy=\"x:90px;y:213px;\"\n\t\t\t\t\t\t\t\tdata-text=\"s:18;l:25;fw:700;\"\n\t\t\t\t\t\t\t\tdata-frame_0=\"y:50px;tp:600;\"\n\t\t\t\t\t\t\t\tdata-frame_1=\"tp:600;e:easeOutExpo;st:900;sp:700;\"\n\t\t\t\t\t\t\t\tdata-frame_999=\"o:0;tp:600;e:nothing;st:w;\"\n\t\t\t\t\t\t\t\tstyle=\"z-index:7;font-family:'lato';\"\n\t\t\t\t\t\t\t>Being different from everyone else<br \/>\nis better than changing to be the same. \n\t\t\t\t\t\t\t<\/rs-layer><!--\n-->\t\t\t\t\t<\/rs-slide>\n\t\t\t\t\t<\/rs-slides>\n\t\t\t\t<\/rs-module>\n\t\t\t\t<script>\n\t\t\t\t\tsetREVStartSize({c: 'rev_slider_14_1',rl:[1240,1024,778,480],el:[],gw:[1349],gh:[508],type:'standard',justify:'',layout:'fullwidth',mh:\"0\"});if (window.RS_MODULES!==undefined && window.RS_MODULES.modules!==undefined && window.RS_MODULES.modules[\"revslider141\"]!==undefined) {window.RS_MODULES.modules[\"revslider141\"].once = false;window.revapi14 = undefined;if (window.RS_MODULES.checkMinimal!==undefined) window.RS_MODULES.checkMinimal()}\n\t\t\t\t<\/script>\n\t\t\t<\/rs-module-wrap>\n\t\t\t<!-- END REVOLUTION SLIDER -->\n<\/div>\n\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t            <\/div>\r\n        <\/div>\r\n        \t\t\t<\/div>\r\n\t\t<\/div>\r\n\t\t\t\t<div class=\"elementor-section elementor-top-section elementor-element elementor-element-74b701a elementor-section-boxed elementor-section-height-default elementor-section-height-default cms-remove-row-no cms-section-no-padding-no cms-boxed-bg-false cms-section-boxed-divider-false cms-overlay-gradient-bg-yes cms-overlay-gradient-mode-tb\" data-id=\"74b701a\" data-element_type=\"section\" data-e-type=\"section\">\r\n\t\t\t<div class=\"cms-overlay-gradient\"><\/div><div class=\"cms-section-boxed-bg\"><\/div><div class=\"cms-section-boxed-divider\"><\/div><div class=\"cms-elementor-section-remove\"><\/div><div class=\"cms-elementor-section-corner cms-elementor-section-corner-top\"><\/div><div class=\"cms-elementor-section-corner cms-elementor-section-corner-bottom\"><\/div>\t\t\t<div class=\"elementor-container elementor-column-gap-default \" >\r\n\t\t\t        <div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-15842bc\" data-id=\"15842bc\" data-element_type=\"column\" data-e-type=\"column\">\r\n            <div class=\"elementor-widget-wrap elementor-element-populated\">\r\n                \t\t<div class=\"elementor-element elementor-element-6932ca9 elementor-widget elementor-widget-heading\" data-id=\"6932ca9\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">ARTICLES AND WHITE PAPERS<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t            <\/div>\r\n        <\/div>\r\n        \t\t\t<\/div>\r\n\t\t<\/div>\r\n\t\t\t\t<div class=\"elementor-section elementor-top-section elementor-element elementor-element-5ed1fa0 elementor-section-boxed elementor-section-height-default elementor-section-height-default cms-remove-row-no cms-section-no-padding-no cms-boxed-bg-false cms-section-boxed-divider-false cms-overlay-gradient-bg-yes cms-overlay-gradient-mode-tb\" data-id=\"5ed1fa0\" data-element_type=\"section\" data-e-type=\"section\">\r\n\t\t\t<div class=\"cms-overlay-gradient\"><\/div><div class=\"cms-section-boxed-bg\"><\/div><div class=\"cms-section-boxed-divider\"><\/div><div class=\"cms-elementor-section-remove\"><\/div><div class=\"cms-elementor-section-corner cms-elementor-section-corner-top\"><\/div><div class=\"cms-elementor-section-corner cms-elementor-section-corner-bottom\"><\/div>\t\t\t<div class=\"elementor-container elementor-column-gap-default \" >\r\n\t\t\t        <div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-f89d279\" data-id=\"f89d279\" data-element_type=\"column\" data-e-type=\"column\">\r\n            <div class=\"elementor-widget-wrap elementor-element-populated\">\r\n                \t\t<div class=\"elementor-element elementor-element-4994145 elementor-widget-divider--view-line elementor-widget elementor-widget-divider\" data-id=\"4994145\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"divider.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<div class=\"elementor-divider\">\n\t\t\t<span class=\"elementor-divider-separator\">\n\t\t\t\t\t\t<\/span>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t            <\/div>\r\n        <\/div>\r\n        \t\t\t<\/div>\r\n\t\t<\/div>\r\n\t\t\t\t<div class=\"elementor-section elementor-top-section elementor-element elementor-element-bd7999a elementor-section-boxed elementor-section-height-default elementor-section-height-default cms-remove-row-no cms-section-no-padding-no cms-boxed-bg-false cms-section-boxed-divider-false cms-overlay-gradient-bg-yes cms-overlay-gradient-mode-tb\" data-id=\"bd7999a\" data-element_type=\"section\" data-e-type=\"section\">\r\n\t\t\t<div class=\"cms-overlay-gradient\"><\/div><div class=\"cms-section-boxed-bg\"><\/div><div class=\"cms-section-boxed-divider\"><\/div><div class=\"cms-elementor-section-remove\"><\/div><div class=\"cms-elementor-section-corner cms-elementor-section-corner-top\"><\/div><div class=\"cms-elementor-section-corner cms-elementor-section-corner-bottom\"><\/div>\t\t\t<div class=\"elementor-container elementor-column-gap-default \" >\r\n\t\t\t        <div class=\"elementor-column elementor-col-50 elementor-top-column elementor-element elementor-element-2aa3eed\" data-id=\"2aa3eed\" data-element_type=\"column\" data-e-type=\"column\">\r\n            <div class=\"elementor-widget-wrap elementor-element-populated\">\r\n                \t\t<div class=\"elementor-element elementor-element-af3e443 elementor-widget elementor-widget-text-editor\" data-id=\"af3e443\" data-element_type=\"widget\" data-e-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\t\t<p>A White Paper initiative was launched by Vantage BioTrials as part of our continued focus and dedication in providing superior clinical trial management services to the pharmaceutical industry. \u00a0Please enjoy reading our free White Papers at your leisure.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t            <\/div>\r\n        <\/div>\r\n                <div class=\"elementor-column elementor-col-50 elementor-top-column elementor-element elementor-element-5f9f656\" data-id=\"5f9f656\" data-element_type=\"column\" data-e-type=\"column\">\r\n            <div class=\"elementor-widget-wrap elementor-element-populated\">\r\n                \t\t<div class=\"elementor-element elementor-element-7845b59 elementor-widget elementor-widget-text-editor\" data-id=\"7845b59\" data-element_type=\"widget\" data-e-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\t\t<p>As part of our commitment, Vantage BioTrials\u2019 White Paper serves to share as an informational resource to give our readers a more detailed look at specific areas of the pharmaceutical\/medical device\/clinical research industry, in addition to providing our own insight and knowledge regarding certain topics, guidelines, practices and policies.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t            <\/div>\r\n        <\/div>\r\n        \t\t\t<\/div>\r\n\t\t<\/div>\r\n\t\t\t\t<div class=\"elementor-section elementor-top-section elementor-element elementor-element-1dfbb29 elementor-section-boxed elementor-section-height-default elementor-section-height-default cms-remove-row-no cms-section-no-padding-no cms-boxed-bg-false cms-section-boxed-divider-false cms-overlay-gradient-bg-yes cms-overlay-gradient-mode-tb\" data-id=\"1dfbb29\" data-element_type=\"section\" data-e-type=\"section\">\r\n\t\t\t<div class=\"cms-overlay-gradient\"><\/div><div class=\"cms-section-boxed-bg\"><\/div><div class=\"cms-section-boxed-divider\"><\/div><div class=\"cms-elementor-section-remove\"><\/div><div class=\"cms-elementor-section-corner cms-elementor-section-corner-top\"><\/div><div class=\"cms-elementor-section-corner cms-elementor-section-corner-bottom\"><\/div>\t\t\t<div class=\"elementor-container elementor-column-gap-default \" >\r\n\t\t\t        <div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-132b871\" data-id=\"132b871\" data-element_type=\"column\" data-e-type=\"column\">\r\n            <div class=\"elementor-widget-wrap elementor-element-populated\">\r\n                \t\t<div class=\"elementor-element elementor-element-14937b3 elementor-widget elementor-widget-html\" data-id=\"14937b3\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"html.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<style>.elementor-accordion .elementor-accordion-item:first-of-type {\ndisplay: none;}\n.elementor-accordion {\n  border-top: 1px solid  #D4DFF2C7;\n}<\/style>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-ab68569 elementor-widget elementor-widget-accordion\" data-id=\"ab68569\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"accordion.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<div class=\"elementor-accordion\">\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-1791\" class=\"elementor-tab-title\" data-tab=\"1\" role=\"button\" aria-controls=\"elementor-tab-content-1791\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\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<a class=\"elementor-accordion-title\" tabindex=\"0\">Perfectly on Time: Successfully Managing Clinical Trial Deliverables<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-1791\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"1\" role=\"region\" aria-labelledby=\"elementor-tab-title-1791\"><p>Publication date: November 2022 \/ Download PDFAuthors: Vatche Bartekian, Johanna Garcia, Sheila Ernest Introduction A key skill for clinical Project Managers (PM) within the life sciences industry is time management. As a PM, you are not only responsible for the project deliverables, but for every person involved as well as every task performed. Yes, it\u2026 <a class=\"mdc-read-more\" href=\"https:\/\/vantagebiotrials.com\/perfectly-on-time-successfully-managing-clinical-trial-deliverables\/\">Read more<\/a><\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-1792\" class=\"elementor-tab-title\" data-tab=\"2\" role=\"button\" aria-controls=\"elementor-tab-content-1792\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\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<a class=\"elementor-accordion-title\" tabindex=\"0\">Why Clinical Trials Fail at the Execution Level<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-1792\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"2\" role=\"region\" aria-labelledby=\"elementor-tab-title-1792\">And how disciplined oversight prevents timeline and data risk\nMost clinical trials do not fail at the level sponsors expect. They fail quietly, during execution, long before endpoints are reached. Not because the science is flawed, but because operational alignment deteriorates across sponsors, CROs, sites &#8230; <a href=\"\/why-clinical-trials-fail-at-the-execution-level\/\">Read more<\/a><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-1793\" class=\"elementor-tab-title\" data-tab=\"3\" role=\"button\" aria-controls=\"elementor-tab-content-1793\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\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<a class=\"elementor-accordion-title\" tabindex=\"0\">Perfectly on Time: Successfully Managing Clinical Trial Deliverables<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-1793\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"3\" role=\"region\" aria-labelledby=\"elementor-tab-title-1793\"><p>A key skill for clinical Project Managers (PM) within the life sciences industry is time management. As a PM, you are not only responsible for the project deliverables, but for every person involved as well as every task performed. Yes, it\u2026 <a class=\"mdc-read-more\" href=\"https:\/\/vantagebiotrials.com\/?p=1105\" data-wplink-edit=\"true\">Read more<\/a><\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-1794\" class=\"elementor-tab-title\" data-tab=\"4\" role=\"button\" aria-controls=\"elementor-tab-content-1794\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\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<a class=\"elementor-accordion-title\" tabindex=\"0\">Planning a Positive Outcome for Your Clinical Trial<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-1794\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"4\" role=\"region\" aria-labelledby=\"elementor-tab-title-1794\"><p>Publication date: September 2022 \/ Download PDFAuthor: Vatche BartekianCo-Authors: Johanna Garcia, Kaiser Lagman, Marina Ohouo,Sheila Ernest Introduction The drug development process presents many complex steps and requires a keen set of skills, knowledge, and resources to arrive successfully at subsequent stages . Within the various phases of drug development, clinical trials, in particular, require robust,\u2026\u00a0<a class=\"mdc-read-more\" href=\"https:\/\/vantagebiotrials.com\/?p=1110\">Read more<\/a><\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-1795\" class=\"elementor-tab-title\" data-tab=\"5\" role=\"button\" aria-controls=\"elementor-tab-content-1795\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\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<a class=\"elementor-accordion-title\" tabindex=\"0\">CRO SELECTION: How to Find & Select the Right Partner for your Clinical Trial<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-1795\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"5\" role=\"region\" aria-labelledby=\"elementor-tab-title-1795\"><p><span style=\"line-height: 22px; color: #333333; font-family: Lato, sans-serif;\">Publication date: January 2021 \/ Download PDF Author: Marc Assaad Introduction As innovation, research and science are exponentially growing in all directions within the healthcare industry, it is only normal that the outsourcing of Clinical Research Organizations (CROs) is also rapidly growing, resulting in a spike in the numbers of such organizations available to\u2026<\/span><span style=\"color: #333333; font-family: Lato, sans-serif;\">\u00a0<\/span><a style=\"background-color: #ffffff; color: #1277a1; transition: all 0.3s ease 0s, visibility 0s ease 0s; display: inline-block; line-height: 22px; font-family: Lato, sans-serif;\" href=\"https:\/\/vantagebiotrials.com\/?p=1115\">Read more<\/a><\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-1796\" class=\"elementor-tab-title\" data-tab=\"6\" role=\"button\" aria-controls=\"elementor-tab-content-1796\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\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<a class=\"elementor-accordion-title\" tabindex=\"0\">Study Rescue | How to get your Clinical Trial Back on Track<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-1796\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"6\" role=\"region\" aria-labelledby=\"elementor-tab-title-1796\"><p><span style=\"line-height: 22px; color: #333333; font-family: Lato, sans-serif;\">Publication date: August 2018 \/ Download PDF Author:\u00a0Han Hsieh \/ Herby Delone Introduction It will probably come as no surprise for anyone to learn that most clinical trials do not proceed as planned since more than 90% of them fail to meet their original timeline.1 The reason a study falls behind schedule or even fails\u2026<\/span><span style=\"color: #333333; font-family: Lato, sans-serif;\">\u00a0<\/span><a class=\"mdc-read-more\" style=\"background-color: #ffffff; color: #1277a1; transition: all 0.3s ease 0s, visibility 0s ease 0s; display: inline-block; line-height: 22px; font-family: Lato, sans-serif;\" href=\"https:\/\/vantagebiotrials.com\/?p=1119\">Read more<\/a><\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-1797\" class=\"elementor-tab-title\" data-tab=\"7\" role=\"button\" aria-controls=\"elementor-tab-content-1797\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\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<a class=\"elementor-accordion-title\" tabindex=\"0\">How to Support & Develop Research \u2013 Na\u00efve Clinical Sites | An Investment for the Future of Clinical Trials<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-1797\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"7\" role=\"region\" aria-labelledby=\"elementor-tab-title-1797\"><p><span style=\"line-height: 22px; color: #333333; font-family: Lato, sans-serif;\">Publication date: January 2018 \/ Download PDF Author:\u00a0Robert Le Introduction Finding highly experienced and strong performing sites for a clinical trial is one of the most important steps in the drug development process, but always remains a challenging task for Sponsors and CROs. The turnover rate of Principle Investigators (PIs) in clinical research is high\u2026<\/span><span style=\"color: #333333; font-family: Lato, sans-serif;\">\u00a0<\/span><a class=\"mdc-read-more\" style=\"background-color: #ffffff; color: #1277a1; transition: all 0.3s ease 0s, visibility 0s ease 0s; display: inline-block; line-height: 22px; font-family: Lato, sans-serif;\" href=\"https:\/\/vantagebiotrials.com\/?p=1096\">Read more<\/a><\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-1798\" class=\"elementor-tab-title\" data-tab=\"8\" role=\"button\" aria-controls=\"elementor-tab-content-1798\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\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<a class=\"elementor-accordion-title\" tabindex=\"0\">Analysis of Highlights from Health Canada\u2019s GCP Inspection Results in 2016<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-1798\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"8\" role=\"region\" aria-labelledby=\"elementor-tab-title-1798\"><p>Publication date: June\u00a02017 \/\u00a0Download as PDF Author:\u00a0Irina Mosesova Introduction At Vantage BioTrials (VBT) we pride ourselves at continuously learning and keeping up to date with the latest developments in clinical research and compliance issues that can potentially effect trial results or even patient safety. The industry is changing at an incredible rate and in an\u2026\u00a0<a class=\"mdc-read-more\" href=\"https:\/\/vantagebiotrials.com\/?p=1099\">Read more<\/a><\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-1799\" class=\"elementor-tab-title\" data-tab=\"9\" role=\"button\" aria-controls=\"elementor-tab-content-1799\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\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<a class=\"elementor-accordion-title\" tabindex=\"0\">A Synthesis of Adaptive Designs in Clinical Trials<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-1799\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"9\" role=\"region\" aria-labelledby=\"elementor-tab-title-1799\"><p>Publication date: May 2016 \/ Download PDF Author: Roy Nitulescu, Agnihotram V Ramanakumar, and Vatch\u00e9 Bartekian Abstract Since 2006, when the adaptive design working group presented their work in Washington D.C., the literature on adaptive designs has greatly expanded. Some designs have emerged as inherently better suited to exploratory-phase trials, while others are more appropriate\u2026\u00a0<a class=\"mdc-read-more\" href=\"https:\/\/vantagebiotrials.com\/?p=1077\">Read more<\/a><\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-17910\" class=\"elementor-tab-title\" data-tab=\"10\" role=\"button\" aria-controls=\"elementor-tab-content-17910\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\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<a class=\"elementor-accordion-title\" tabindex=\"0\">Quality by Design in Clinical Research<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-17910\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"10\" role=\"region\" aria-labelledby=\"elementor-tab-title-17910\"><p>In clinical research, \u201chigh quality\u201d means that a study generates good, useful data, does not harm the study participants, and proceeds smoothly with few interruptions by errors or omissions. However, too many clinical research studies get mired in a time-consuming quality control (QC) process that generates numerous site monitor findings (e.g., missing data, ineligible study participants, other protocol deviations), data queries, and other after-the-fact indications that a quality problem has been found and needs to be fixed. A research site may be unable to deliver acceptable results, no matter how much the sponsor tries to help. In severe cases, the design of a study incorporates problems that make it impossible to achieve high quality results, no matter how well the study is conducted.\u00a0<a class=\"mdc-read-more\" href=\"https:\/\/vantagebiotrials.com\/?p=1059\">Read more<\/a><\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-17911\" class=\"elementor-tab-title\" data-tab=\"11\" role=\"button\" aria-controls=\"elementor-tab-content-17911\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\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<a class=\"elementor-accordion-title\" tabindex=\"0\">Clinical Trial Management: Houston, We Have a Problem<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-17911\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"11\" role=\"region\" aria-labelledby=\"elementor-tab-title-17911\"><p>In the management of clinical trials, whether they be local, international, multi-site, simple or complex, a variety of situations can (or should I say will) occur that will have you saying \u201cHouston, we have a problem!\u201d These complications may be related to an issue at the clinical site itself, within the CRO or at the Sponsor level, but could also be caused by the study protocol or the investigational drug itself. This white paper will present a methodology to optimize clinical trial management by using best practices, as well as how to avoid and resolve problematic situations that may arise throughout the trial.\u00a0<a class=\"mdc-read-more\" href=\"https:\/\/vantagebiotrials.com\/?p=1092\">Read more<\/a><\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-17912\" class=\"elementor-tab-title\" data-tab=\"12\" role=\"button\" aria-controls=\"elementor-tab-content-17912\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\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<a class=\"elementor-accordion-title\" tabindex=\"0\">Quality by Design and Risk-Based Monitoring<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-17912\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"12\" role=\"region\" aria-labelledby=\"elementor-tab-title-17912\"><p>Over the past decade, the clinical research industry\u2019s standard to meet regulatory monitoring obligations has involved frequent and regular onsite monitoring visits with 100% source data verification (SDV). The belief that \u201cmore is better\u201d continues even with new evidence that on-site monitoring practices do not necessarily guarantee patient safety and data quality. An electronic survey was conducted by the Clinical Trials Transformation Initiative (CTTI) in 2008 to assess the clinical monitoring practices utilized across different types of organizations involved in clinical research. The results published in 2011 have highlighted the heterogeneity in monitoring practices between clinical trial organizations, and the key conclusion is that traditional monitoring is inefficient and doesn\u2019t always lead to increased patient safety and data quality in clinical trials.\u00a0<a class=\"mdc-read-more\" href=\"https:\/\/vantagebiotrials.com\/?p=1082\">Read more<\/a><\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-17913\" class=\"elementor-tab-title\" data-tab=\"13\" role=\"button\" aria-controls=\"elementor-tab-content-17913\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\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<a class=\"elementor-accordion-title\" tabindex=\"0\">Prioritizing Agility When Choosing a Contract Research Organization<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-17913\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"13\" role=\"region\" aria-labelledby=\"elementor-tab-title-17913\"><p>Publication date: September 2023 \/ Download PDFAuthor: Jos\u00e9e Comeau Introduction Throughout the years, the field of clinical research has continued to grow in complexity and has encountered numerous challenges, and although processes have been well established, many of us have settled into a daily routine that maintains the status quo. It\u2019s time for us to\u2026 <a class=\"mdc-read-more\" href=\"https:\/\/vantagebiotrials.com\/?p=1042\">Read more<\/a><\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-17914\" class=\"elementor-tab-title\" data-tab=\"14\" role=\"button\" aria-controls=\"elementor-tab-content-17914\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\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<a class=\"elementor-accordion-title\" tabindex=\"0\">Criteria for Choosing a Great Contract Research Organization (CRO)<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-17914\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"14\" role=\"region\" aria-labelledby=\"elementor-tab-title-17914\"><div class=\"panel-heading active\"><p class=\"panel-title\">\u00a0<a title=\"Criteria for Choosing a Great Contract Research Organization (CRO)\" href=\"https:\/\/vantagebiotrials.com\/criteria-for-choosing-a-great-contract-research-organization-cro\/\">Criteria for Choosing a Great Contract Research Organization (CRO)<\/a><\/p><p>Publication date: February 2024 \/ Download PDF Author: Yiken Bartekian Introduction Outsourcing is often necessary within the health care industry. Many pharmaceutical biotechnology and medical devic ecompanies rely on outsourcing to Contract Research Organizations (CRO&#8217;s) as part of their strategy to advance to the next stage of clinical trials. As a matter of perspective, the&#8230; <a href=\"https:\/\/vantagebiotrials.com\/?p=1456\">Read More<\/a><\/p><\/div><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t<script type=\"application\/ld+json\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@type\":\"FAQPage\",\"mainEntity\":[{\"@type\":\"Question\",\"name\":\"Perfectly on Time: Successfully Managing Clinical Trial Deliverables\",\"acceptedAnswer\":{\"@type\":\"Answer\",\"text\":\"<p>Publication date: November 2022 \\\/ Download PDFAuthors: Vatche Bartekian, Johanna Garcia, Sheila Ernest Introduction A key skill for clinical Project Managers (PM) within the life sciences industry is time management. As a PM, you are not only responsible for the project deliverables, but for every person involved as well as every task performed. Yes, it\\u2026 <a class=\\\"mdc-read-more\\\" href=\\\"https:\\\/\\\/vantagebiotrials.com\\\/perfectly-on-time-successfully-managing-clinical-trial-deliverables\\\/\\\">Read more<\\\/a><\\\/p>\"}},{\"@type\":\"Question\",\"name\":\"Why Clinical Trials Fail at the Execution Level\",\"acceptedAnswer\":{\"@type\":\"Answer\",\"text\":\"And how disciplined oversight prevents timeline and data risk\\nMost clinical trials do not fail at the level sponsors expect. They fail quietly, during execution, long before endpoints are reached. Not because the science is flawed, but because operational alignment deteriorates across sponsors, CROs, sites &#8230; <a href=\\\"\\\/why-clinical-trials-fail-at-the-execution-level\\\/\\\">Read more<\\\/a>\"}},{\"@type\":\"Question\",\"name\":\"Perfectly on Time: Successfully Managing Clinical Trial Deliverables\",\"acceptedAnswer\":{\"@type\":\"Answer\",\"text\":\"<p>A key skill for clinical Project Managers (PM) within the life sciences industry is time management. As a PM, you are not only responsible for the project deliverables, but for every person involved as well as every task performed. Yes, it\\u2026 <a class=\\\"mdc-read-more\\\" href=\\\"https:\\\/\\\/vantagebiotrials.com\\\/?p=1105\\\" data-wplink-edit=\\\"true\\\">Read more<\\\/a><\\\/p>\"}},{\"@type\":\"Question\",\"name\":\"Planning a Positive Outcome for Your Clinical Trial\",\"acceptedAnswer\":{\"@type\":\"Answer\",\"text\":\"<p>Publication date: September 2022 \\\/ Download PDFAuthor: Vatche BartekianCo-Authors: Johanna Garcia, Kaiser Lagman, Marina Ohouo,Sheila Ernest Introduction The drug development process presents many complex steps and requires a keen set of skills, knowledge, and resources to arrive successfully at subsequent stages . Within the various phases of drug development, clinical trials, in particular, require robust,\\u2026\\u00a0<a class=\\\"mdc-read-more\\\" href=\\\"https:\\\/\\\/vantagebiotrials.com\\\/?p=1110\\\">Read more<\\\/a><\\\/p>\"}},{\"@type\":\"Question\",\"name\":\"CRO SELECTION: How to Find & Select the Right Partner for your Clinical Trial\",\"acceptedAnswer\":{\"@type\":\"Answer\",\"text\":\"<p><span style=\\\"line-height: 22px; color: #333333; font-family: Lato, sans-serif;\\\">Publication date: January 2021 \\\/ Download PDF Author: Marc Assaad Introduction As innovation, research and science are exponentially growing in all directions within the healthcare industry, it is only normal that the outsourcing of Clinical Research Organizations (CROs) is also rapidly growing, resulting in a spike in the numbers of such organizations available to\\u2026<\\\/span><span style=\\\"color: #333333; font-family: Lato, sans-serif;\\\">\\u00a0<\\\/span><a style=\\\"background-color: #ffffff; color: #1277a1; transition: all 0.3s ease 0s, visibility 0s ease 0s; display: inline-block; line-height: 22px; font-family: Lato, sans-serif;\\\" href=\\\"https:\\\/\\\/vantagebiotrials.com\\\/?p=1115\\\">Read more<\\\/a><\\\/p>\"}},{\"@type\":\"Question\",\"name\":\"Study Rescue | How to get your Clinical Trial Back on Track\",\"acceptedAnswer\":{\"@type\":\"Answer\",\"text\":\"<p><span style=\\\"line-height: 22px; color: #333333; font-family: Lato, sans-serif;\\\">Publication date: August 2018 \\\/ Download PDF Author:\\u00a0Han Hsieh \\\/ Herby Delone Introduction It will probably come as no surprise for anyone to learn that most clinical trials do not proceed as planned since more than 90% of them fail to meet their original timeline.1 The reason a study falls behind schedule or even fails\\u2026<\\\/span><span style=\\\"color: #333333; font-family: Lato, sans-serif;\\\">\\u00a0<\\\/span><a class=\\\"mdc-read-more\\\" style=\\\"background-color: #ffffff; color: #1277a1; transition: all 0.3s ease 0s, visibility 0s ease 0s; display: inline-block; line-height: 22px; font-family: Lato, sans-serif;\\\" href=\\\"https:\\\/\\\/vantagebiotrials.com\\\/?p=1119\\\">Read more<\\\/a><\\\/p>\"}},{\"@type\":\"Question\",\"name\":\"How to Support & Develop Research \\u2013 Na\\u00efve Clinical Sites | An Investment for the Future of Clinical Trials\",\"acceptedAnswer\":{\"@type\":\"Answer\",\"text\":\"<p><span style=\\\"line-height: 22px; color: #333333; font-family: Lato, sans-serif;\\\">Publication date: January 2018 \\\/ Download PDF Author:\\u00a0Robert Le Introduction Finding highly experienced and strong performing sites for a clinical trial is one of the most important steps in the drug development process, but always remains a challenging task for Sponsors and CROs. The turnover rate of Principle Investigators (PIs) in clinical research is high\\u2026<\\\/span><span style=\\\"color: #333333; font-family: Lato, sans-serif;\\\">\\u00a0<\\\/span><a class=\\\"mdc-read-more\\\" style=\\\"background-color: #ffffff; color: #1277a1; transition: all 0.3s ease 0s, visibility 0s ease 0s; display: inline-block; line-height: 22px; font-family: Lato, sans-serif;\\\" href=\\\"https:\\\/\\\/vantagebiotrials.com\\\/?p=1096\\\">Read more<\\\/a><\\\/p>\"}},{\"@type\":\"Question\",\"name\":\"Analysis of Highlights from Health Canada\\u2019s GCP Inspection Results in 2016\",\"acceptedAnswer\":{\"@type\":\"Answer\",\"text\":\"<p>Publication date: June\\u00a02017 \\\/\\u00a0Download as PDF Author:\\u00a0Irina Mosesova Introduction At Vantage BioTrials (VBT) we pride ourselves at continuously learning and keeping up to date with the latest developments in clinical research and compliance issues that can potentially effect trial results or even patient safety. The industry is changing at an incredible rate and in an\\u2026\\u00a0<a class=\\\"mdc-read-more\\\" href=\\\"https:\\\/\\\/vantagebiotrials.com\\\/?p=1099\\\">Read more<\\\/a><\\\/p>\"}},{\"@type\":\"Question\",\"name\":\"A Synthesis of Adaptive Designs in Clinical Trials\",\"acceptedAnswer\":{\"@type\":\"Answer\",\"text\":\"<p>Publication date: May 2016 \\\/ Download PDF Author: Roy Nitulescu, Agnihotram V Ramanakumar, and Vatch\\u00e9 Bartekian Abstract Since 2006, when the adaptive design working group presented their work in Washington D.C., the literature on adaptive designs has greatly expanded. Some designs have emerged as inherently better suited to exploratory-phase trials, while others are more appropriate\\u2026\\u00a0<a class=\\\"mdc-read-more\\\" href=\\\"https:\\\/\\\/vantagebiotrials.com\\\/?p=1077\\\">Read more<\\\/a><\\\/p>\"}},{\"@type\":\"Question\",\"name\":\"Quality by Design in Clinical Research\",\"acceptedAnswer\":{\"@type\":\"Answer\",\"text\":\"<p>In clinical research, \\u201chigh quality\\u201d means that a study generates good, useful data, does not harm the study participants, and proceeds smoothly with few interruptions by errors or omissions. However, too many clinical research studies get mired in a time-consuming quality control (QC) process that generates numerous site monitor findings (e.g., missing data, ineligible study participants, other protocol deviations), data queries, and other after-the-fact indications that a quality problem has been found and needs to be fixed. A research site may be unable to deliver acceptable results, no matter how much the sponsor tries to help. In severe cases, the design of a study incorporates problems that make it impossible to achieve high quality results, no matter how well the study is conducted.\\u00a0<a class=\\\"mdc-read-more\\\" href=\\\"https:\\\/\\\/vantagebiotrials.com\\\/?p=1059\\\">Read more<\\\/a><\\\/p>\"}},{\"@type\":\"Question\",\"name\":\"Clinical Trial Management: Houston, We Have a Problem\",\"acceptedAnswer\":{\"@type\":\"Answer\",\"text\":\"<p>In the management of clinical trials, whether they be local, international, multi-site, simple or complex, a variety of situations can (or should I say will) occur that will have you saying \\u201cHouston, we have a problem!\\u201d These complications may be related to an issue at the clinical site itself, within the CRO or at the Sponsor level, but could also be caused by the study protocol or the investigational drug itself. This white paper will present a methodology to optimize clinical trial management by using best practices, as well as how to avoid and resolve problematic situations that may arise throughout the trial.\\u00a0<a class=\\\"mdc-read-more\\\" href=\\\"https:\\\/\\\/vantagebiotrials.com\\\/?p=1092\\\">Read more<\\\/a><\\\/p>\"}},{\"@type\":\"Question\",\"name\":\"Quality by Design and Risk-Based Monitoring\",\"acceptedAnswer\":{\"@type\":\"Answer\",\"text\":\"<p>Over the past decade, the clinical research industry\\u2019s standard to meet regulatory monitoring obligations has involved frequent and regular onsite monitoring visits with 100% source data verification (SDV). The belief that \\u201cmore is better\\u201d continues even with new evidence that on-site monitoring practices do not necessarily guarantee patient safety and data quality. An electronic survey was conducted by the Clinical Trials Transformation Initiative (CTTI) in 2008 to assess the clinical monitoring practices utilized across different types of organizations involved in clinical research. The results published in 2011 have highlighted the heterogeneity in monitoring practices between clinical trial organizations, and the key conclusion is that traditional monitoring is inefficient and doesn\\u2019t always lead to increased patient safety and data quality in clinical trials.\\u00a0<a class=\\\"mdc-read-more\\\" href=\\\"https:\\\/\\\/vantagebiotrials.com\\\/?p=1082\\\">Read more<\\\/a><\\\/p>\"}},{\"@type\":\"Question\",\"name\":\"Prioritizing Agility When Choosing a Contract Research Organization\",\"acceptedAnswer\":{\"@type\":\"Answer\",\"text\":\"<p>Publication date: September 2023 \\\/ Download PDFAuthor: Jos\\u00e9e Comeau Introduction Throughout the years, the field of clinical research has continued to grow in complexity and has encountered numerous challenges, and although processes have been well established, many of us have settled into a daily routine that maintains the status quo. It\\u2019s time for us to\\u2026 <a class=\\\"mdc-read-more\\\" href=\\\"https:\\\/\\\/vantagebiotrials.com\\\/?p=1042\\\">Read more<\\\/a><\\\/p>\"}},{\"@type\":\"Question\",\"name\":\"Criteria for Choosing a Great Contract Research Organization (CRO)\",\"acceptedAnswer\":{\"@type\":\"Answer\",\"text\":\"<div class=\\\"panel-heading active\\\"><p class=\\\"panel-title\\\">\\u00a0<a title=\\\"Criteria for Choosing a Great Contract Research Organization (CRO)\\\" href=\\\"https:\\\/\\\/vantagebiotrials.com\\\/criteria-for-choosing-a-great-contract-research-organization-cro\\\/\\\">Criteria for Choosing a Great Contract Research Organization (CRO)<\\\/a><\\\/p><p>Publication date: February 2024 \\\/ Download PDF Author: Yiken Bartekian Introduction Outsourcing is often necessary within the health care industry. Many pharmaceutical biotechnology and medical devic ecompanies rely on outsourcing to Contract Research Organizations (CRO&#8217;s) as part of their strategy to advance to the next stage of clinical trials. As a matter of perspective, the&#8230; <a href=\\\"https:\\\/\\\/vantagebiotrials.com\\\/?p=1456\\\">Read More<\\\/a><\\\/p><\\\/div>\"}}]}<\/script>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t            <\/div>\r\n        <\/div>\r\n        \t\t\t<\/div>\r\n\t\t<\/div>\r\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>ARTICLES AND WHITE PAPERS A White Paper initiative was launched by Vantage BioTrials as part of our continued focus and dedication in providing superior clinical trial management services to the pharmaceutical industry. \u00a0Please enjoy reading our free White Papers at your leisure. As part of our commitment, Vantage BioTrials\u2019 White Paper serves to share as an informational resource to give our readers a more detailed look at specific areas of the pharmaceutical\/medical device\/clinical research industry, in addition to providing our own insight and knowledge regarding certain topics, guidelines, practices and policies. Perfectly on Time: Successfully Managing Clinical Trial Deliverables Publication date: November 2022 \/ Download PDFAuthors: Vatche Bartekian, Johanna Garcia, Sheila Ernest Introduction A key skill for clinical Project Managers (PM) within the life sciences industry is time management. As a PM, you are not only responsible for the project deliverables, but for every person involved as well as every task performed. Yes, it\u2026 Read more Why Clinical Trials Fail at the Execution Level And how disciplined oversight prevents timeline and data risk Most clinical trials do not fail at the level sponsors expect. They fail quietly, during execution, long before endpoints are reached. Not because the science is flawed, but because operational alignment deteriorates across sponsors, CROs, sites &#8230; Read more Perfectly on Time: Successfully Managing Clinical Trial Deliverables A key skill for clinical Project Managers (PM) within the life sciences industry is time management. As a PM, you are not only responsible for the project deliverables, but for every person involved as well as every task performed. Yes, it\u2026 Read more Planning a Positive Outcome for Your Clinical Trial Publication date: September 2022 \/ Download PDFAuthor: Vatche BartekianCo-Authors: Johanna Garcia, Kaiser Lagman, Marina Ohouo,Sheila Ernest Introduction The drug development process presents many complex steps and requires a keen set of skills, knowledge, and resources to arrive successfully at subsequent stages . Within the various phases of drug development, clinical trials, in particular, require robust,\u2026\u00a0Read more CRO SELECTION: How to Find &#038; Select the Right Partner for your Clinical Trial Publication date: January 2021 \/ Download PDF Author: Marc Assaad Introduction As innovation, research and science are exponentially growing in all directions within the healthcare industry, it is only normal that the outsourcing of Clinical Research Organizations (CROs) is also rapidly growing, resulting in a spike in the numbers of such organizations available to\u2026\u00a0Read more Study Rescue | How to get your Clinical Trial Back on Track Publication date: August 2018 \/ Download PDF Author:\u00a0Han Hsieh \/ Herby Delone Introduction It will probably come as no surprise for anyone to learn that most clinical trials do not proceed as planned since more than 90% of them fail to meet their original timeline.1 The reason a study falls behind schedule or even fails\u2026\u00a0Read more How to Support &#038; Develop Research \u2013 Na\u00efve Clinical Sites | An Investment for the Future of Clinical Trials Publication date: January 2018 \/ Download PDF Author:\u00a0Robert Le Introduction Finding highly experienced and strong performing sites for a clinical trial is one of the most important steps in the drug development process, but always remains a challenging task for Sponsors and CROs. The turnover rate of Principle Investigators (PIs) in clinical research is high\u2026\u00a0Read more Analysis of Highlights from Health Canada\u2019s GCP Inspection Results in 2016 Publication date: June\u00a02017 \/\u00a0Download as PDF Author:\u00a0Irina Mosesova Introduction At Vantage BioTrials (VBT) we pride ourselves at continuously learning and keeping up to date with the latest developments in clinical research and compliance issues that can potentially effect trial results or even patient safety. The industry is changing at an incredible rate and in an\u2026\u00a0Read more A Synthesis of Adaptive Designs in Clinical Trials Publication date: May 2016 \/ Download PDF Author: Roy Nitulescu, Agnihotram V Ramanakumar, and Vatch\u00e9 Bartekian Abstract Since 2006, when the adaptive design working group presented their work in Washington D.C., the literature on adaptive designs has greatly expanded. Some designs have emerged as inherently better suited to exploratory-phase trials, while others are more appropriate\u2026\u00a0Read more Quality by Design in Clinical Research In clinical research, \u201chigh quality\u201d means that a study generates good, useful data, does not harm the study participants, and proceeds smoothly with few interruptions by errors or omissions. However, too many clinical research studies get mired in a time-consuming quality control (QC) process that generates numerous site monitor findings (e.g., missing data, ineligible study participants, other protocol deviations), data queries, and other after-the-fact indications that a quality problem has been found and needs to be fixed. A research site may be unable to deliver acceptable results, no matter how much the sponsor tries to help. In severe cases, the design of a study incorporates problems that make it impossible to achieve high quality results, no matter how well the study is conducted.\u00a0Read more Clinical Trial Management: Houston, We Have a Problem In the management of clinical trials, whether they be local, international, multi-site, simple or complex, a variety of situations can (or should I say will) occur that will have you saying \u201cHouston, we have a problem!\u201d These complications may be related to an issue at the clinical site itself, within the CRO or at the Sponsor level, but could also be caused by the study protocol or the investigational drug itself. This white paper will present a methodology to optimize clinical trial management by using best practices, as well as how to avoid and resolve problematic situations that may arise throughout the trial.\u00a0Read more Quality by Design and Risk-Based Monitoring Over the past decade, the clinical research industry\u2019s standard to meet regulatory monitoring obligations has involved frequent and regular onsite monitoring visits with 100% source data verification (SDV). The belief that \u201cmore is better\u201d continues even with new evidence that on-site monitoring practices do not necessarily guarantee patient safety and data quality. An electronic survey was conducted by the Clinical Trials Transformation Initiative (CTTI) in 2008 to assess the clinical monitoring practices utilized across different types of organizations involved in clinical research. The results published in 2011 have highlighted the heterogeneity in monitoring practices between clinical trial organizations, and the key conclusion is that traditional monitoring is inefficient and doesn\u2019t always lead to increased patient safety and data quality in clinical trials.\u00a0Read more Prioritizing Agility When Choosing a Contract Research Organization Publication date: September 2023 \/ Download PDFAuthor: Jos\u00e9e Comeau Introduction Throughout the years, the field of clinical research has continued to grow in complexity and has encountered numerous challenges, and although processes have been well established, many of us have settled into a daily routine that maintains the status quo. It\u2019s time for us to\u2026 Read more Criteria for Choosing a Great Contract Research Organization (CRO) \u00a0Criteria for Choosing a Great Contract Research Organization (CRO) Publication date: February 2024 \/ Download PDF Author: Yiken Bartekian Introduction Outsourcing is often necessary within the health care industry. Many pharmaceutical biotechnology and medical devic ecompanies rely on outsourcing to Contract Research Organizations (CRO&#8217;s) as part of their strategy to advance to the next stage of clinical trials. As a matter of perspective, the&#8230; Read More<\/p>","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"om_disable_all_campaigns":false,"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"class_list":["post-50","page","type-page","status-publish","hentry","cms-no-post-thumbnail"],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/vantagebiotrials.com\/fr\/wp-json\/wp\/v2\/pages\/50","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/vantagebiotrials.com\/fr\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/vantagebiotrials.com\/fr\/wp-json\/wp\/v2\/types\/page"}],"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=50"}],"version-history":[{"count":3,"href":"https:\/\/vantagebiotrials.com\/fr\/wp-json\/wp\/v2\/pages\/50\/revisions"}],"predecessor-version":[{"id":4997,"href":"https:\/\/vantagebiotrials.com\/fr\/wp-json\/wp\/v2\/pages\/50\/revisions\/4997"}],"wp:attachment":[{"href":"https:\/\/vantagebiotrials.com\/fr\/wp-json\/wp\/v2\/media?parent=50"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}