SterlingBio Shares Insight on Regulatory Document Management for Clinical Study Electronic Trial Master Files at DIA Annual Meeting in Washington D.C.

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SterlingBio to Share Insight on Regulatory Document Management for Electronic Trial Master Files at DIA 46th Annual Meeting in Washington D.C. Industry Leading Clinical Research Organization to Showcase Solutions and Strategies for Ensuring Regulatory Document Compliance and Document Management.

SterlingBio to Share Insight on Regulatory Document Management for Electronic Trial Master Files at DIA 46th Annual Meeting in Washington D.C. Industry Leading Clinical Research Organization to Showcase Solutions and Strategies for Ensuring Regulatory Document Compliance and Document Management.

News Facts
Building on its commitment to help health sciences organizations discover, develop and market innovative products and services, SterlingBio will have a significant presence at the DIA 46th Annual Meeting in Washington, D.C., June 13-17, 2010.

SterlingBio’s booth (#2322) will feature an interactive demonstration of SterlingBio’s Java and Oracle web-based solution for clinical trial electronic trial master file document management, SureTrial™, and clinical data integration with Oracle Health Sciences, Documentum and other sources of electronic healthcare applications data. SterlingBio’s web-based solution, SureTrial eTMF™, helps pharmaceutical firms convert paper-based health sciences data to electronic information for use in regulated drug development efforts.

DIA 2010 attendees and individuals following the conference remotely can stay updated on SterlingBio news and insights from the conference by following http://www.SterlingBio.com

Oracle, Java, Documentum and SureTrial are registered trademarks of Oracle and/or its affiliates. Other names may be trademarks of their respective owners.

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Zack Schmidt
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