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

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