The Opportunities and Challenges of Risk Management Compliance in Medical Device Engineering

 

When executed well, risk management provides opportunities for product innovation, as well as reducing costs of defects and rework. However, when executed inefficiently Risk Management compliance can bog down development and result in increased regulatory scrutiny. Our panelists will present strategies for leveraging risk management efficiently and effectively to create opportunities to reduce costs and improve quality while also demonstrating compliance. The presentations will then be followed by a panel discussion on challenges medical device manufacturers commonly face when complying to ISO 14971.

Date: September 20, 2011
Time: 12PM CT | 1PM ET
Webcast Duration: 60 minutes


Speakers:

Ryan Lloyd


Ryan Lloyd
Director, Medical Devices Market Strategy
PTC


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Edwin L. Bills


Edwin L. Bills
Principal Consultant
Bilanx Consulting LLC


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Thomas R. Varricchione


Thomas R. Varricchione, RRT, MBA
Principal Advisor, Clinical and Regulatory Affairs
Ximedica, Incorporated


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Moderator:


Heather Thompson
Editor-in-Chief
MD&DI


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