Clinical trials
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Documentum is a leading provider of enterprise content management (ECM) solutions, specifically tailored for the highly regulated life sciences, pharmaceutical, and healthcare industries. Now a part of OpenText, the platform offers a suite of applications designed to manage the entire lifecycle of regulated content, including clinical trial documentation (eTMF), regulatory submissions (eCTD), and quality management systems (QMS). Its services help organizations maintain compliance with global standards such as FDA 21 CFR Part 11 and EMA regulations. The platform is widely used by major pharmaceutical companies to streamline research and development workflows and ensure data integrity across the drug development process.
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