Webinar Date: March 11, 2010 Time: 1:00 to 1:30 PST
Summary:
With a significant portion of the data needed for regulatory submissions resident in ECM systems, the desire to integrate content management systems with regulatory submissions continues to increase. USDM has a depth of experience in working with both technology providers, and in helping FDA regulated companies in building efficiencies and best practice for integrating ECM with regulatory submissions.
Sponsored By USDM's ECM Practice Learn More
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USDM is a leading global consulting firm focused on life sciences. We specialize in regulated business processes, with an emphasis on compliance and performance.
USDM provides innovative services and solutions that enable life science companies to achieve and maintain compliance across the entire enterprise.