Software Design for Medical Devices Europe 2011
January 19 - 21, 2011
慕尼黑 , 德国
Ensuring Compliance to Evolving Regulatory Standards and Incorporating Quality and Efficiency into Design
Software Design for Medical Devices Europe is the only pan-European conference that focuses on the important area of software design in the Medical Device industry. The event will address the key issues in development, regulation and compliance including:
Adapting effectively to the 2010 changes to the EU Medical Device Directive to reduce the risk of compliance failure and streamline new submissions
Getting the latest updates from the perspective of the Notified Bodies, including TUV and Underwriters Laboratories - just how can you get your product on to the market quicker?
Hear from the FDA what precisely their expectations are in order to get approval and how their Guidance is changing, including their stance on IEC 62304 and 93/42/eec integration
Software Design for Medical Devices Europe is the only pan-European conference that focuses on the important area of software design in the Medical Device industry. The event will address the key issues in development, regulation and compliance including:
Adapting effectively to the 2010 changes to the EU Medical Device Directive to reduce the risk of compliance failure and streamline new submissions
Getting the latest updates from the perspective of the Notified Bodies, including TUV and Underwriters Laboratories - just how can you get your product on to the market quicker?
Hear from the FDA what precisely their expectations are in order to get approval and how their Guidance is changing, including their stance on IEC 62304 and 93/42/eec integration
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