CIMdata PLM Industry Summary Online Archive
15 November 2005
Company News
MatrixOne and Possis Medical to Present Best Practices for Managing FDA Regulation Compliance Throughout Product Development
With medical devices facing new regulation requirements from the FDA's 21 CFR Part 11 and Part 820 mandates, MatrixOne, Inc. announced that it will present a webcast on how managing product information electronically can significantly ease compliance efforts. Possis Medical, a manufacturer of advanced medical devices for the large and growing cardiovascular and vascular treatment market, will co-present on how the company leverages MatrixOne's integrated PLM FDA compliance solution in its business processes.
Companies currently using paper-based systems to meet FDA requirements are putting themselves at risk and a competitive disadvantage. The electronic workflow provided by PLM can streamline quality assurance and compliance, while helping to improve profitability through faster time-to-market.
"MatrixOne PLM provides immediate access to information, improves productivity throughout the product development process, captures data necessary for regulatory compliance, facilitates multidisciplinary collaboration and captures critical corporate knowledge," said Tim Anderson, director of engineering for Possis Medical. "The technology is a big step for us in our corporate strategy for growing our business in the years to come and introducing innovative life-saving products."
What : Free webcast entitled "Managing Regulatory Compliance Throughout Product Development"
When : Wednesday, November 16, 2005 at 1:00 pm ET
Who : Barry Foster, product director, MatrixOne; George Schmidt, senior PLM business consultant, MatrixOne; Rob Oveson, manager, documentation systems configuration, Possis Medical; Tim Anderson, director of engineering, Possis Medical
Where : For additional information on this event or to register, please visit http://www.matrixone.com/plmlive/live.html .
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