CIMdata PLM Industry Summary Online Archive
4 January 2010
Events News
Omnify Software Hosts Webinar on Conducting an FDA/ISO Compliant Validation
What: Medical Device FDA/ISO Compliance Webinar.
With a growing number of regulations, Medical Device manufacturers need a simplified way to achieve compliance while maintaining efficient product development. One approach many manufacturers take is to utilize Product Lifecycle Management (PLM) technology in order to automate processes and create a controlled environment for managing all of the information involved in designing their products. However, industry regulators require that the technology be validated to confirm compliance to the written standards.
This webinar will demonstrate how PLC Medical Systems, a leader in technologies for the Cardiac and Vascular Markets, automated Engineering Change and Training Processes with PLM technology for continuous improvement. In addition, attendees will see how the company designed and executed a validation protocol to meet various FDA (Food and Drug Administration) and ISO (International Organization for Standardization) compliance requirements.
Who: Jeff Steward, Director of IT and Ern Damon, Document Control Manager for PLC Medical Systems, David Solimini, Vice President of Technical Sales for Omnify Software
When: Wednesday, February 3, 2010, 1:30 P.M. EST
Where: Event will be presented online; those interested in attending this event can register at:
http://www.omnifysoft.com/Register/Default.aspx?type=7
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