•  

Case Study: Understanding the Changes within IEC 60601 3rd Edition and Developing an Efficient Compliance and Implementation Str

A session at 2nd Annual Software Design for Medical Devices Europe

  • Reviewing the 2010 amendments to the directive
  • Discussing best practices for integrating these new requirements into product development
  • Understanding the realistic impact on both your business and your engineers
  • Assessing the expectations of regulators and notified bodies in terms of new submissions

Sign in to add slides, notes or videos to this session

Tell your friends!

View the schedule

Share

See something wrong?

Report an issue with this session