CIMdata PLM Industry Summary Online Archive
1 August 2007
Events News
PTC To Host Executive Seminar: Achieving Regulatory Compliance, Improving Product Quality, And Reducing Time-To-Market
PTC announced that it will host a seminar designed to provide medical device companies with actionable recommendations on how to achieve success in their compliance initiatives, shorten development cycles and improve product quality. The complimentary hour long webcast will feature presentations from Christine Nelson, former Quality Systems expert and director of international affairs, FDA CDRH, David Rubin, director, medical device market strategy, PTC, and Bob DiNitto, vice president, quality assurance & regulatory affairs, Alva MedTech Consulting..
The panel of experts will discuss the regulations governing the industry and describe the tools necessary to help medical device manufacturers improve quality, shorten development cycles, reduce time to market and improve regulatory compliance. The panel will also share case studies highlighting medical device companies that have achieved these benefits by leveraging product lifecycle management (PLM) solutions to improve their product development processes
Topics include:
• Quality System Inspection Technique (QSIT)
• What the FDA looks for in the 21 CFR Part 820 Design Control subsystem
• Satisfying 21 CFR Part 11
• Hardwiring compliance into your product development process
• Accelerating your product development process
• Case studies demonstrating how medical device companies have reduced the length and improved the quality and compliance of their new product development process
Date and time: August 16, 2007 11:00 am - 12:00 PM EST
To register, please visit http://www.ptc.com/go/med_device or call +1 734.997.0200.
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