  {"id":14601,"date":"2017-02-06T12:50:14","date_gmt":"2017-02-06T11:50:14","guid":{"rendered":"http:\/\/www.veeva.com\/eu\/?post_type=resources&#038;p=14601"},"modified":"2026-06-20T00:17:48","modified_gmt":"2026-06-19T22:17:48","slug":"veeva-submissions-publishing","status":"publish","type":"resources","link":"https:\/\/www.veeva.com\/eu\/resources\/veeva-submissions-publishing\/","title":{"rendered":"³Ô¹Ï±¬ÁÏ Submissions Publishing"},"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}<\/p>\n<p>.veeva-2024 .content-block__content .stat-box {\nbackground: #eef1f5;\ndisplay: inline-block;\npadding: 10px 30px;\nborder-radius: 16px;\nfont-size: 18px;\nmargin: 5px 5px 20px 5px;\nfont-weight: 500;\n}\n.veeva-2024 .content-block__content .stat-box span {\ncolor:#f5670e;\nfont-weight:600;\n}\n\/* to remove the mobile dropdown *\/\n.veeva-2024 .form-dropdown {\ndisplay: none;\n}<\/p>\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\/10\/veeva-submissions-publishing-features-brief-figure-one.png\"><\/p>\n<h2>Continuous publishing on a unified RIM platform<\/h2>\n<p><img decoding=\"async\" class=\"img-right d-block d-lg-none\" alt=\"\" src=\"https:\/\/www.veeva.com\/wp-content\/uploads\/2025\/10\/veeva-submissions-publishing-features-brief-figure-one.png\"><\/p>\n<p>Traditional publishing processing activities are sequential and disjointed. Companies often rely on multiple technologies including document management systems, publishing tools, and spreadsheets for planning and tracking submissions. Each gap between systems introduces inefficiencies and delays.<\/p>\n<p>³Ô¹Ï±¬ÁÏ Submissions Publishing is a continuous publishing solution within the ³Ô¹Ï±¬ÁÏ RIM Platform that dramatically speeds up submission delivery. It eliminates the need for standalone publishing software and manual document exchanges between fragmented systems. Users can complete publishing tasks, including cross-document hyperlinking and validation, earlier in the process when issues are easier to fix. This avoids multiple rounds of unnecessary internal reviews.<\/p>\n<p>Used in conjunction with ³Ô¹Ï±¬ÁÏ Submissions and ³Ô¹Ï±¬ÁÏ Submissions Archive, ³Ô¹Ï±¬ÁÏ Submissions Publishing streamlines end-to-end publishing processes to drive greater automation, transparency, and speed.<\/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>\n<p><strong>Faster submission preparation process.<\/strong><\/p>\n<p>Publishing in parallel with authoring while consolidating and automating workflows eliminates redundant steps.<\/p>\n<\/li>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Better control and end-to-end view.<\/strong><\/p>\n<p>Authors and publishers collaborate side-by- side in the same tool with a holistic, consistent view of the entire process.<\/p>\n<\/li>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Trusted quality.<\/strong><\/p>\n<p>Viewing documents in their final context while they are still in draft reduces the risk of errors and content re-work.<\/p>\n<\/li>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Unified RIM.<\/strong><\/p>\n<p>Connect end-to-end regulatory processes and improve efficiency as part of the ³Ô¹Ï±¬ÁÏ RIM Platform.<\/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>\n<p><strong>Assisted Submission Building<\/strong><\/p>\n<p>Eliminate manual steps with rule-based auto-matching. Leverage documents and metadata from submission content plans.<\/p>\n<\/li>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Submission Independent Hyperlinking<\/strong><\/p>\n<p>Create hyperlinks that are independent of the submission structure so they can be used earlier in the process during document reviews and reused across multiple submissions.<\/p>\n<\/li>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Background Validation<\/strong><\/p>\n<p>Automate validation and link testing with a tool that identifies problems as submissions are being built.<\/p>\n<\/li>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Submission-ready Rendering<\/strong><\/p>\n<p>Automatically render all documents with the correct PDF standards. Navigate web links, cross-references, and tables of contents directly from the viewer.<\/p>\n<\/li>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Real-time Status Reporting<\/strong><\/p>\n<p>Gain visibility into the complete submission process including submission status and individual document readiness.<\/p>\n<\/li>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Gateway Integration<\/strong><\/p>\n<p>Transfer submissions through health authority electronic submission gateways, automatically archiving all gateway receipts and responses.<\/p>\n<\/li>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>eCTD Support <\/strong><\/p>\n<p>Stay compliant with global eCTD and non- eCTD standards.<\/p>\n<\/li>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Granular Document Merging <\/strong><\/p>\n<p>Merge submission-ready documents across an entire content plan or part of the content plan to meet agency requirements.<\/p>\n<\/li>\n<\/ul>\n<p><img decoding=\"async\" class=\"img-responsive\" alt=\"\" src=\"https:\/\/www.veeva.com\/wp-content\/uploads\/2025\/10\/veeva-submissions-publishing-features-brief-figure-two.png\"><\/p>\n<h2>³Ô¹Ï±¬ÁÏ RIM<\/h2>\n<p>³Ô¹Ï±¬ÁÏ Submissions Publishing is part of ³Ô¹Ï±¬ÁÏ RIM, which streamlines global regulatory processes on a single, cloud-based platform. This enables life sciences companies to:<\/p>\n<ul>\n<li>Ensure teams are developing reliable regulatory content with high data integrity<\/li>\n<li>Coordinate regulatory efforts across headquarters, affiliates, and partners<\/li>\n<li>Respond faster to changing regulations<\/li>\n<li>Increase end-to-end process efficiency from submission planning to publishing<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>³Ô¹Ï±¬ÁÏ Submissions Publishing incorporates publishing functionality within the ³Ô¹Ï±¬ÁÏ RIM Suite to provide end-to-end submission development on a single platform.<\/p>\n","protected":false},"featured_media":0,"parent":0,"template":"","class_list":["post-14601","resources","type-resources","status-publish","hentry","resource-do-not-display-do-not-display","resource-social-hide-social-icons","resource-area-20-regulatory","resource-product-20-submissions","resource-type-product-briefs"],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/www.veeva.com\/eu\/wp-json\/wp\/v2\/resources\/14601"}],"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":5,"href":"https:\/\/www.veeva.com\/eu\/wp-json\/wp\/v2\/resources\/14601\/revisions"}],"predecessor-version":[{"id":86632,"href":"https:\/\/www.veeva.com\/eu\/wp-json\/wp\/v2\/resources\/14601\/revisions\/86632"}],"wp:attachment":[{"href":"https:\/\/www.veeva.com\/eu\/wp-json\/wp\/v2\/media?parent=14601"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}