{"id":63633,"date":"2022-04-06T13:26:48","date_gmt":"2022-04-06T11:26:48","guid":{"rendered":"http:\/\/www.veeva.com\/eu\/?post_type=resources&#038;p=63633"},"modified":"2026-01-27T15:10:12","modified_gmt":"2026-01-27T14:10:12","slug":"submission-content-plans-feature-brief","status":"publish","type":"resources","link":"https:\/\/pantheon.veeva.com\/eu\/resources\/submission-content-plans-feature-brief\/","title":{"rendered":"Submission Content Plans Feature Brief"},"content":{"rendered":"<style>\n.veeva-2024 .fa-ul li p {\nmargin-top:5px;\n}\n.veeva-2024 .content-block .fa-check-circle {\ncolor: #f7981d;\nfont-weight: 400;\nfont-size:20px;\n}\n@media (min-width:768px) {\n.veeva-2024 .hero-centered {\npadding: 100px 0;\n}\n}\n@media (min-width:992px) {\n.veeva-2024 .content-block {\nmargin-top: 6rem;\n}\n}\n.veeva-2024 .content-block__sidebar {\ndisplay: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\/2025\/06\/submission-content-plans-resource-figure-1.png\"><\/p>\n<h2>Simplify submission content planning, management, and compilation to save significant time and effort<\/h2>\n<p>Veeva RIM Submission Content Plans (SCPs) provide a unique, structured, and collaborative approach to planning, tracking, and managing submission development. As the volume of submissions continues to grow, regulatory teams need a way to track submission development across multiple markets. Many companies are using multiple tools for this work, including Excel, Microsoft Project, emails, and file shares. With SCPs, teams can efficiently plan, track, and develop all content required for submissions in a single, collaborative space.<\/p>\n<p><img decoding=\"async\" class=\"img-right d-block d-lg-none\" alt=\"\" src=\"https:\/\/www.veeva.com\/wp-content\/uploads\/2025\/06\/submission-content-plans-resource-figure-1.png\"><\/p>\n<h2>Business Benefits<\/h2>\n<ul class=\"fa-ul\">\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span><br \/>\n   <strong>Increase submission efficiency.<\/strong><\/p>\n<p>Streamline communication and task delegation with a single source of truth, while reducing duplicative tasks and manual data entry with templates and automation.<\/p>\n<\/li>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span><br \/>\n  <strong>Transparent global submission statuses.<\/strong><\/p>\n<p>Gain a holistic, real-time, view of individual document and submission progress across submission teams and markets.<\/p>\n<\/li>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span><br \/>\n   <strong>Enhanced compliance.<\/strong><\/p>\n<p>Improve global traceability of submitted documents, including what versions were submitted to which Health Authorities, and where to find the latest source documents when it\u2019s time to make an update.<\/p>\n<\/li>\n<\/ul>\n<h2>Features<\/h2>\n<ul class=\"fa-ul\">\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span><br \/>\n   <strong>Content plan templates <\/strong><\/p>\n<p>Leverage our recommended constraints to standardize submission planning by submission type, product, or region.<\/p>\n<\/li>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span><br \/>\n  <strong>Content plan viewer<\/strong><\/p>\n<p>Plan submissions, collaborate on content assembly, and track progress to completion using a holistic view that can be easily tailored to each user\u2019s preference.<\/p>\n<\/li>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span><br \/>\n   <strong>Advanced document matching<\/strong><\/p>\n<p>Reduce manual tasks with Veeva\u2019s most recent improvements to automated and suggested matching for documents.<\/p>\n<\/li>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span><br \/>\n   <strong>Drag-and-drop documents<\/strong><\/p>\n<p>Drag and drop RIM documents from your library, or external files from your desktop for automated assignment and document upload.<\/p>\n<\/li>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span><br \/>\n   <strong>Real-time reports and dashboards<\/strong><\/p>\n<p>Automate status reporting on progress, tasks, and timelines with real-time dashboards and reports. Easily report on which documents have been submitted to which Health Authorities.<\/p>\n<\/li>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span><br \/>\n   <strong>Foundation for Continuous Innovation<\/strong><\/p>\n<p>SCPs is a prerequisite for adopting more of Veeva RIM\u2019s high value features, including Active Dossier, Global Content Planning and Veeva Publishing.<\/p>\n<\/li>\n<\/ul>\n<h2>Veeva RIM <\/h2>\n<p>Submission Content Plans (SCPs) are a capability within Veeva RIM that streamlines submission preparation on a single, cloud-based platform. SCPs enable companies to:<\/p>\n<ul>\n<li>Develop reliable regulatory content with high data integrity<\/li>\n<li>Coordinate regulatory efforts across internal teams, affiliates, partners, and regions<\/li>\n<li>Increase end-to-end process efficiency from submission planning to publishing<\/li>\n<\/ul>\n<p>Learn more about how <a href=\"\/eu\/products\/veeva-submissions\/\">Veeva Submissions<\/a> can streamline your global regulatory submission process. <\/p>\n","protected":false},"excerpt":{"rendered":"<p>Submission content plans help streamline submission content planning, document creation and collection, and plan completion 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