{"id":98647,"date":"2026-06-12T22:26:07","date_gmt":"2026-06-12T20:26:07","guid":{"rendered":"https:\/\/www.veeva.com\/eu\/?post_type=resources&#038;p=98647"},"modified":"2026-06-22T17:05:40","modified_gmt":"2026-06-22T15:05:40","slug":"veeva-study-training-gcp-product-brief","status":"publish","type":"resources","link":"https:\/\/pantheon.veeva.com\/eu\/resources\/veeva-study-training-gcp-product-brief\/","title":{"rendered":"Trial-Ready GCP Training for Sponsors, Sites, and CROs"},"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>\nDrive ICH GCP E6(R3) compliance with trial-ready courses maintained by Veeva. This includes a standalone GCP course recognized by TransCelerate, as well as additional accredited courses for further GCP learning.\n<\/p>\n<p>\nAutomatically assign GCP training across sponsor, site, and CRO personnel in Veeva Study Training. Plus, enable site staff to demonstrate GCP training completion across sponsors to reduce repetitive training.\n<\/p>\n<h3>Benefits<\/h3>\n<ul class=\"fa-ul\">\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Drive GCP compliance<\/strong> with tailored courses recognized by TransCelerate BioPharma. <\/li>\n<\/p>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Future-proof your training<\/strong> with Veeva-managed <a href=\"https:\/\/www.learngxp.com\/\" target=\"_blank\" rel=\"noreferrer noopener\">courses<\/a> that evolve with regulatory updates.<\/li>\n<\/p>\n<li><span class=\"fa-li\"><i class=\"far fa-check-circle\"><\/i><\/span>\n<p><strong>Streamline training<\/strong> by assigning courses automatically through Veeva Study Training.\n<\/li>\n<\/p>\n<\/ul>\n<h3>Courses<\/h3>\n<p><strong>Standalone course for GCP compliance<\/strong><\/p>\n<ul>\n<li><a href=\"https:\/\/www.learngxp.com\/elearning\/veeva-gcp-for-clinical-trials\/\" target=\"_blank\" rel=\"noreferrer noopener\">Veeva GCP for Clinical Trials<\/a> (45 minutes)<\/li>\n<\/ul>\n<p><strong>Additional courses<\/strong><\/p>\n<ul>\n<li><a href=\"https:\/\/www.learngxp.com\/elearning\/general-principles-of-good-clinical-practices\/\" target=\"_blank\" rel=\"noreferrer noopener\">ICH E6(R3) &#8211; General Principles of GCP<\/a> (20 minutes)<\/li>\n<li><a href=\"https:\/\/www.learngxp.com\/elearning\/ich-e6-r3-sponsor\/\" target=\"_blank\" rel=\"noreferrer noopener\">ICH E6(R3) &#8211; Sponsor<\/a> (25 minutes)<\/li>\n<li><a href=\"https:\/\/www.learngxp.com\/elearning\/data-governance\/\" target=\"_blank\" rel=\"noreferrer noopener\">ICH E6(R3) &#8211; Data Governance<\/a> (15 minutes)<\/li>\n<li><a href=\"https:\/\/www.learngxp.com\/elearning\/ich-e6-r3-investigator\/\" target=\"_blank\" rel=\"noreferrer noopener\">ICH E6(R3) &#8211; Investigator<\/a> (10 minutes)<\/li>\n<li><a href=\"https:\/\/www.learngxp.com\/elearning\/ich-e6-r3-irb-iec\/\" target=\"_blank\" rel=\"noreferrer noopener\">ICH E6(R3) &#8211; IRB\/IEC<\/a> (15 minutes)<\/li>\n<li><a href=\"https:\/\/www.learngxp.com\/elearning\/ich-e6-r3-appendices\/\" target=\"_blank\" rel=\"noreferrer noopener\">ICH E6(R3) &#8211; Appendices<\/a> (15 minutes)<\/li>\n<li><a href=\"https:\/\/www.learngxp.com\/elearning\/investigator-oversight-of-clinical-trials\/\" target=\"_blank\" rel=\"noreferrer noopener\">Investigator Oversight of Clinical Trials<\/a> (15 minutes)<\/li>\n<li><a href=\"https:\/\/www.learngxp.com\/elearning\/informed-consent\/\" target=\"_blank\" rel=\"noreferrer noopener\">Informed Consent<\/a> (15 minutes)<\/li>\n<li><a href=\"https:\/\/www.learngxp.com\/elearning\/clinical-trial-safety-reporting\/\" target=\"_blank\" rel=\"noreferrer noopener\">Clinical Trial Safety Reporting<\/a> (10 minutes)<\/li>\n<li><a href=\"https:\/\/www.learngxp.com\/elearning\/the-fundamentals-of-recist-1-1\/\" target=\"_blank\" rel=\"noreferrer noopener\">Fundamentals of RECIST 1.1<\/a> (15 minutes)<\/li>\n<\/ul>\n<hr>\n<h3>About Veeva Study Training<\/h3>\n<p>\n<a href=\"https:\/\/www.veeva.com\/eu\/products\/veeva-study-training\/\">Veeva Study Training<\/a> brings sponsors, CROs, and research sites into a single platform to streamline and automate training while ensuring inspection readiness.\n<\/p>\n<h3>About Veeva LearnGxP<\/h3>\n<p>\nWith <a href=\"https:\/\/www.learngxp.com\/\" target=\"_blank\" rel=\"noreferrer noopener\">Veeva LearnGxP\u2019s<\/a> accredited GxP training library, organizations can significantly reduce deviations, reclaim valuable workforce time, and eliminate the burden of creating training in-house. View our course catalog.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Learn how to leverage trial-ready GCP courses in Veeva Study Training and drive ICH GCP E6(R3) compliance.<\/p>\n","protected":false},"featured_media":98649,"parent":0,"template":"","class_list":["post-98647","resources","type-resources","status-publish","has-post-thumbnail","hentry","resource-area-20-clinical-operations","resource-product-20-study-training","resource-type-product-briefs","region-eu"],"aioseo_notices":[],"aioseo_head":"\n\t\t<!-- All in One SEO Pro 5.0.1 - aioseo.com -->\n\t<meta name=\"description\" content=\"Learn how to leverage trial-ready GCP courses in Veeva Study Training and drive ICH GCP E6(R3) compliance.\" \/>\n\t<meta name=\"robots\" content=\"max-image-preview:large\" \/>\n\t<link rel=\"canonical\" href=\"https:\/\/pantheon.veeva.com\/eu\/resources\/veeva-study-training-gcp-product-brief\/\" \/>\n\t<meta name=\"generator\" content=\"All in One SEO Pro (AIOSEO) 5.0.1\" 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