Documentum announced the introduction of an ECM Solution for Life Sciences. This new offering is designed to meet the specialized content management requirements of biotechnology, pharmaceutical and medical device companies; clinical research and contract manufacturing organizations (CRO/CMO); and governing bodies that regulate these industries. The new solution is a combination of Documentum and partner products, best practices, shared standards, project templates, and consulting services. Based on Documentum’s core ECM technology, the solution enables lifecycle control of all documents, such as new drug applications (NDAs); auditing of content creation, revision and approvals to ensure regulatory compliance; sharing and reuse of project-related content for team collaboration in product development and clinical trials. The solution also supports cross-organizational collaboration. The Documentum ECM for Life Sciences automates and streamlines: R&D Content Management, Operations Content Management, and Marketing Content Management. Documentum will provide consulting services, guidance on industry best practices and industry-specific project templates and accelerators. The Documentum Life Sciences Solution is available immediately.