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

The conference will take place 19-21 January 2011 at Le Meridien in Munich, Germany.