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Sparta Systems, Inc. Partners with Documentum to Provide Customers Best of Breed Solutions for Quality Management and Electronic Content Management HOLMDEL, N.J., Nov. 11 /PRNewswire/ -- Sparta Systems, Inc., the market leader in enterprise Quality Management Systems (QMS), and makers of TrackWise(R) software, announced today that it has partnered with Documentum , the leading provider of enterprise content management (ECM). Initially targeting the quality arena for FDA-regulated industries, Sparta Systems will be providing a host of integrated solutions based on the Documentum-ECM platform. "By providing collaborative applications, we aim to enable organizations to achieve dynamic collaboration in QMS and electronic document management across their enterprises," noted Ran Flam, President & CEO at Sparta Systems. Sparta Systems will be releasing an integrated TrackWise-Documentum ECM solution that will enable users to perform Documentum functions directly from TrackWise. Customers will be able to link files and file versions stored in Documentum directly to quality records in TrackWise. Further capabilities will enable users to perform other document management functions directly from the TrackWise application, such as reserve, unreserve, add new content, or create new versions. This provides a "one stop shop" for companies who are looking to implement EDM software in addition to QMS software. "The integrated combination QMS built on the Documentum ECM platform provides a level of IT consolidation and productivity efficiency that many organizations seek," said Barry Ruditsky, vice president of OEM and VAR channels for Documentum. "IT can leverage the convenience of a common infrastructure or framework, and apply common corporate rules across the board. Users will enjoy the efficiency of a solution that works the way their business process flows. We are pleased to have Sparta Systems as a member of our ISV partner community." About Sparta Systems, Inc. Sparta Systems has positioned itself as a leader in providing 21 CFR Part 11 compliant, off-the-shelf, fully user-configurable solutions for the management and tracking of discrepancies, nonconformances, investigations, customer complaints, audit observations, regulatory commitments, corrective and preventive actions (CAPA), change authorizations, and other cGxP requirements by FDA-regulated companies, specifically in the pharmaceutical, biotechnology, and medical device industries. Sparta Systems has over 85 FDA- regulated customers, including most of the major pharmaceutical manufacturers. DATASOURCE: Sparta Systems, Inc. CONTACT: Steve Cagle, Manager, Operations, Sparta Systems, +1-732-203-0400 ext 121 or Web site: http://www.sparta-systems.com/

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