{"id":78249,"date":"2024-07-12T23:15:25","date_gmt":"2024-07-12T21:15:25","guid":{"rendered":"https:\/\/www.veeva.com\/eu\/?page_id=78249"},"modified":"2026-07-02T11:54:03","modified_gmt":"2026-07-02T09:54:03","slug":"why-every-biopharma-needs-a-ctms","status":"publish","type":"page","link":"https:\/\/pantheon.veeva.com\/eu\/why-every-biopharma-needs-a-ctms\/","title":{"rendered":"Better Trials, Better Outcomes:\u2028Why Every Biopharma Needs a CTMS"},"content":{"rendered":"<div class=\"product-banner-hero\" style=\"background-image: url('https:\/\/www.veeva.com\/wp-content\/uploads\/2024\/06\/CTMS-hero-2000x450@2x.png');\">\n<div class=\"container\">\n<div class=\"row\">\n<div class=\"hidden-xs col-xs-12\">\n\t\t\t<\/div>\n<div class=\"row banner-flex-align\">\n<div class=\"col-sm-12 text-left\">\n<h1>Why Every Biopharma<br \/> Needs a CTMS<\/h1>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"product-container\">\n<div class=\"container\">\n<div class=\"row text-left\">\n<div class=\"col-12 col-md-11 col-lg-10 col-centered\">\n<h2 class=\"text-center fake-h1\">Better Trials, Better Outcomes: <br \/>Why Every Biopharma Needs a CTMS<\/h2>\n<p>\n\t\t\t\t\tManaging the growing complexity and cost of clinical trials requires strong operational controls. A robust clinical trial management system (CTMS) delivers this control across both insourced and outsourced study models, streamlining operations to accelerate trial completion and regulatory submission.\n\t\t\t\t<\/p>\n<p>\n\t\t\t\t\tThis comprehensive guide will explore how a CTMS can help you take control of your trials regardless of your operating model. We&#8217;ll dive into the challenges of managing clinical trials without a centralized system and share how a CTMS:\n\t\t\t\t<\/p>\n<ul>\n<li>Improves efficiency and reduces errors with automated workflows and centralized data management<\/li>\n<li>Fosters seamless communication and data sharing between internal teams and CROs<\/li>\n<li>Improves study oversight to lower risks of data quality problems and serious compliance gaps<\/li>\n<li>Enables data-driven decision-making with comprehensive reporting and analytics<\/li>\n<\/ul><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"product-container\" style=\"padding-top:0;padding-bottom:100px;\">\n<div class=\"container\">\n<div class=\"row\">\n<div class=\"col-12 col-md-11 col-lg-10 col-centered\">\n<div class=\"text-center\" style=\"border-radius: 50px;background: #F1F3F6;padding:40px 40px 20px 40px\">\n<h2 class=\"mt-15 mb-50\">What is your clinical trial operating model?<\/h2>\n<div class=\"row\">\n<div class=\"col-md-6\">\n<img decoding=\"async\" style=\"width:56px\" src=\"https:\/\/www.veeva.com\/wp-content\/uploads\/2024\/06\/CTMS-icon-outsource@2x.png\" alt=\"\" \/><\/p>\n<h2 class=\"mt-25 mb-30\">My team <strong>outsources<\/strong><br \/> most clinical trial<br \/> activities to a CRO.<\/h2>\n<div class=\"veeva-2024 mb-40\"><a href=\"\/eu\/resources\/outsourcing-clinical-trial-activities-without-sacrificing-study-oversight\/\" style=\"display:inline-block\" class=\"button-primary button-primary--gradient\" target=\"_self\" rel=\"noopener\">Show Me More<\/a><\/div>\n<\/p><\/div>\n<div class=\"col-md-6\">\n\t\t\t\t\t\t\t<img decoding=\"async\" style=\"width:56px\" src=\"https:\/\/www.veeva.com\/wp-content\/uploads\/2024\/06\/CTMS-icon-in-house@2x.png\" alt=\"\" \/><\/p>\n<h2 class=\"mt-25 mb-30\">My team performs most<br \/> clinical trial activities<br \/> <strong>in-house.<\/strong><\/h2>\n<div class=\"veeva-2024 mb-20\"><a href=\"\/eu\/resources\/streamlining-in-house-trial-management-with-a-modern-ctms\/\" style=\"display:inline-block\" class=\"button-primary button-primary--gradient\" target=\"_self\" rel=\"noopener\">Show Me More<\/a><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"modal white fade\" id=\"form-modal1\" style=\"display: none;\" aria-hidden=\"true\">\n<div class=\"modal-win-content\">\n<div class=\"modal-dialog modal-xl\">\n<div class=\"mod-close\">\n\t\t\t\t<a href=\"#\" class=\"glyph-link\"><\/a>\n\t\t\t<\/div>\n<div class=\"products-form-shadow text-center\">\n<p>\t\t\t\t<iframe loading=\"lazy\" src=\"https:\/\/go.veeva.com\/l\/28972\/2024-06-18\/9pz4j1\" width=\"100%\" height=\"600\" frameborder=\"0\" style=\"border: 0\"><\/iframe>\n\t\t\t<\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"modal white fade\" id=\"form-modal2\" style=\"display: none;\" aria-hidden=\"true\">\n<div class=\"modal-win-content\">\n<div class=\"modal-dialog modal-xl\">\n<div class=\"mod-close\">\n\t\t\t\t<a href=\"#\" class=\"glyph-link\"><\/a>\n\t\t\t<\/div>\n<div class=\"products-form-shadow text-center\">\n<p>\t\t\t\t<iframe loading=\"lazy\" src=\"https:\/\/go.veeva.com\/l\/28972\/2024-06-18\/9pz4j7\" width=\"100%\" height=\"620\" frameborder=\"0\" style=\"border: 0\"><\/iframe>\n\t\t\t<\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Groundbreaking research conducted through clinical trials propels medical advancements. Managing these trials, however, is a costly and complex endeavor.<\/p>\n","protected":false},"author":42,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"templates\/template-full-page.php","meta":{"footnotes":"","_members_access_role":[],"_members_access_error":""},"coauthors":[1699],"class_list":["post-78249","page","type-page","status-publish","hentry","page_type-hub"],"aioseo_notices":[],"aioseo_head":"\n\t\t<!-- All in One SEO Pro 5.0.1 - aioseo.com -->\n\t<meta name=\"description\" content=\"Why Every Biopharma Needs a CTMS Better Trials, Better Outcomes: Why Every Biopharma Needs a CTMS Managing the growing complexity and cost of clinical trials requires strong operational controls. 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