Managing Life Cycle Requirements for Developing and Maintaining Medical Device Software per IEC 62304

Complying with the IEC 62304 standard to produce safe and effective medical devices requires that software design and development follows defined and controlled processes. This demands hardware and software teams to establish a common set of systems requirements, develop software with proper verifications, risk management, and maintain traceability. This is the third in the series on IEC62304 webinars that will take a deeper dive into managing requirements, modeling, testing, verification, and maintaining traceability throughout the product life cycle. It will demonstrate the power of team collaboration, and efficiency of re-usability to produce high quality reliable products, with lower costs and faster cycle times, that are safe, effective and compliant with regulations.

Date: June 23, 2011
Time:12 Noon CT | 1PM ET
Webcast Duration: 60 minutes


Speakers:

Suresh Wadhwani


Suresh Wadhwani
Consulting Technical Specialist
IBM Rational


For more information about our speaker, please click here.

Deric Merino Bio


Deric Merino
Rational Specialty Architect
IBM Rational


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Moderator:

Rich Nass

Rich Nass
Director of Content
UBM Canon Medical Device Media Group


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