Drive Efficiency. Enhance Usability. Improve Visibility and Insight.
The EMC® Documentum® for Life Sciences solution suite breaks down information silos to transform how organizations access, manage and share regulated content. Doing so provides a single source of accurate, complete, and compliant content reduces risk, and helps bring high quality, safe products to market faster at a lower cost.
Documentum eTMF - What's New! What's Next!
Watch this webcast and hear Adam Kelch, Senior Product Manager, Documentum Clinical Solutions, provide an overview of the key enhancements of Documentum eTMF announced at EMC World in Las Vegas in May. He’ll also discuss how our latest release (4.2) delivers more granular eTMF planning, better quality and actionable insight.
Documentum for Life Sciences Regulatory Solutions - What's New! What's Next!
Listen as Lena Shafir, Product Manager, Life Sciences Regulatory Solutions, provides an overview of recent enhancements to Documentum Research and Development (R&D) and Documentum Store and View (SSV). She’ll also cover how our latest release (4.2) delivers lifecycle support for medical device documentation and ensures alignment with global regulatory guidance to speed submissions.
Documentum Quality and Manufacturing (Q&M) - What's New! What's Next!
Hear Jessica Kelley, Quality Product Manager, provide an overview of the key enhancements and integrations with Documentum Q&M announced at EMC World in Las Vegas in May. She’ll also explain how our latest release (4.2) delivers lifecycle support for medical device documentation from design to production manufacturing and provides flexible print controls to maximize efficiency while ensuring compliance.