{"id":12861,"date":"2016-07-08T14:13:44","date_gmt":"2016-07-08T12:13:44","guid":{"rendered":"http:\/\/www.veeva.com\/eu\/?post_type=resources&#038;p=12861"},"modified":"2026-03-17T21:24:16","modified_gmt":"2026-03-17T20:24:16","slug":"veeva-vault-study-startup-product-brief","status":"publish","type":"resources","link":"https:\/\/www.veeva.com\/eu\/resources\/veeva-vault-study-startup-product-brief\/","title":{"rendered":"³Ô¹Ï±¬ÁÏ Study Startup Features Brief"},"content":{"rendered":"<style>\n.veeva-2024 .fa-ul li p {\n  margin-top: 5px;\n}\n.veeva-2024 .content-block .fa-check-circle {\n  color: #f7981d;\n  font-weight: 400;\n  font-size: 20px;\n}\n@media (min-width: 768px) {\n  .veeva-2024 .hero-centered {\n    padding: 100px 0;\n  }\n}\n@media (min-width: 992px) {\n  .veeva-2024 .content-block {\n    margin-top: 6rem;\n  }\n}\n.veeva-2024 .content-block__sidebar {\n  display: none;\n}\n<\/style>\n<p><img decoding=\"async\" class=\"img-right d-none d-lg-block\" alt=\"\" src=\"https:\/\/www.veeva.com\/wp-content\/uploads\/2016\/07\/Study-Startup-FB-Img-1.png\"><\/p>\n<h2>End-to-End Study Start-Up in One Application<\/h2>\n<p>\n³Ô¹Ï±¬ÁÏ Study Startup accelerates time to site activation by connecting global teams and enabling best practices for managing country and site start-up processes.\n<\/p>\n<p>\nBecause study start-up documentation and data (including milestone information, baseline, projected, and actual dates) are managed in a single system, sponsors and CROs have early visibility to bottlenecks associated with events on the critical path to activation. As a result, resources can be more efficiently allocated and adjusted based on start-up progress.\n<\/p>\n<h3 style=\"color:orange\">Business Benefits<\/h3>\n<ul class=\"fa-ul\">\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Speed study start-up.<\/strong><br \/>\nStreamline end-to-end study start-up processes &#8211; from site identification to site greenlight &#8211; to accelerate time to site activation.<\/li>\n<\/p>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Make better, more informed decisions.<\/strong><br \/>\nActively monitor and track site activation progress with realtime dashboards and reports.<\/li>\n<\/p>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Enable effective collaboration.<\/strong><br \/>\nAchieve greater alignment across study partners through seamless exchange of start-up content and information.<\/li>\n<\/p>\n<\/ul>\n<h3 style=\"color:orange\">Features<\/h3>\n<ul class=\"fa-ul\">\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Site Feasibility and Selection<\/strong><br \/>\nEasily collect investigator and facility data to make better decisions about sites that should be qualified. Distribute feasibility surveys automatically to qualifying sites for easy completion and tracking. Site selection workflows automatically trigger downstream activation activities for seamless start-up management and visibility.\n<\/li>\n<\/p>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Contract and Budget Lifecycles<\/strong><br \/>\nStreamline the contracting process by leveraging a dedicated Contracts and Budgets lifecycle. Calculate cycle times to monitor the timeliness of negotiations, assisting with better planning and faster negotiations in future studies.<\/li>\n<\/p>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Standard Questions and Reusable Responses<\/strong><br \/>\nMake survey completion easier for sites by shortening surveys and saving and pre-populating responses with ³Ô¹Ï±¬ÁÏ-supported industry-standard questions.<\/li>\n<\/p>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Submissions Tracking<\/strong><br \/>\nSimplify submissions and track key dates, statuses, and documents needed for Health Authority submissions and Ethics Committee submissions, including EU CTR and RFI tracking. Take advantage of a productized connector with ³Ô¹Ï±¬ÁÏ RIM for alignment between Regulatory and Clinical teams.<\/li>\n<\/p>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Study Startup Homepage<\/strong><br \/>\nPrioritize and manage critical tasks and milestones, including high-priority, overdue, and at-risk activities, across multiple studies through a visually intuitive homepage. Start-up specialists and managers get a quick snapshot of start-up progress, can drill down into underlying details, and take immediate action directly from the homepage.<\/li>\n<\/p>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Global Milestones and Standard Metrics<\/strong><br \/>\nMeasure cycle times and get visibility into key performance indicators to identify areas for improvement and optimize startup processes.<\/li>\n<\/p>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Global Workflows and Country Intelligence<\/strong><br \/>\n³Ô¹Ï±¬ÁÏ Study Startup specialists gain full visibility into progress across countries, tracking sites, and required documents to quickly identify blockers to a site\u2019s greenlight. Submission workflows ensure completeness before regulatory handoff. With 45+ built-in country workflows, teams can efficiently navigate complex country startup requirements.<\/li>\n<\/p>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Unified Clinical Operations Platform<\/strong><br \/>\n³Ô¹Ï±¬ÁÏ Study Startup shares documentation and data with other core Clinical products without complex integrations. Milestones and tasks are populated in ³Ô¹Ï±¬ÁÏ CTMS. Start-up teams can automatically exchange essential documents with sites via ³Ô¹Ï±¬ÁÏ Site Connect based on country-specific tailored lists, and start-up content is auto-filled in ³Ô¹Ï±¬ÁÏ eTMF.<\/li>\n<\/p>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Study Startup Milestones<\/strong><br \/>\nActivities and documents required for site activation are linked to study milestones, defining the critical path to open a country and get every site to the first subject and first visit faster.<\/li>\n<\/p>\n<\/ul>\n<hr>\n<h2>About ³Ô¹Ï±¬ÁÏ Clinical Operations<\/h2>\n<p>\n<strong style=\"color:orange\">³Ô¹Ï±¬ÁÏ Clinical Operations<\/strong> empowers clinical teams with a unified platform for efficient trial execution. Streamlined processes and improved data visibility from startup through closeout accelerates timelines and enhances collaboration across sponsors, sites, and CROs.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Learn how to accelerate site activation. <\/p>\n","protected":false},"featured_media":12929,"parent":0,"template":"","class_list":["post-12861","resources","type-resources","status-publish","has-post-thumbnail","hentry","resource-social-hide-social-icons","resource-area-20-clinical-operations","resource-product-20-study-startup","resource-type-product-briefs"],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/www.veeva.com\/eu\/wp-json\/wp\/v2\/resources\/12861"}],"collection":[{"href":"https:\/\/www.veeva.com\/eu\/wp-json\/wp\/v2\/resources"}],"about":[{"href":"https:\/\/www.veeva.com\/eu\/wp-json\/wp\/v2\/types\/resources"}],"version-history":[{"count":4,"href":"https:\/\/www.veeva.com\/eu\/wp-json\/wp\/v2\/resources\/12861\/revisions"}],"predecessor-version":[{"id":53185,"href":"https:\/\/www.veeva.com\/eu\/wp-json\/wp\/v2\/resources\/12861\/revisions\/53185"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.veeva.com\/eu\/wp-json\/wp\/v2\/media\/12929"}],"wp:attachment":[{"href":"https:\/\/www.veeva.com\/eu\/wp-json\/wp\/v2\/media?parent=12861"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}