Webinar Date: May 27, 2010 Time: 11:00 to 11:30 PST
Summary:
How does the regulated life science company make this dream a reality? Automated data collection, operator work instruction execution, and electronic batch record reporting for cGMP operations can simplify, unify and optimize the manufacturing environment of the life science organization. We will explore the integration of manufacturing execution and electronic batch record systems with ERP. Both technologies as well as accepted methodologies have advanced in recent years unveiling opportunity for life sciences companies to cost effectively achieve automation on the manufacturing floor that which creates increased efficiency and compliance in the enterprise resource planning business processes.
Please join us on Thursday, May 27, 2010 to explore:
Sponsored By: USDM's ERP 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.