IEC 62304 for Medical Device Software Development: Steps to Compliance - Webinar By GlobalCompliancePanel 2012

  • 19 Jul 2012
  • Webinar

Description

IEC 62304 for Medical Device Software Development: Steps to Compliance is a webinar that covers topics such as:

  • How to write meaningful requirements
  • Software requirements specification
  • Multi software system implementation
  • Software architectures
  • Requirements traceability
  • Software design documentation
  • Software testing in real-time systems
  • Software unit and integration testing
  • SOUP (software of unknown providence)
  • Software tools

IEC 62304 for Medical Device Software Development: Steps to Compliance brings together Regulatory / Quality Control, Project Management and Software Engineering.

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Important

Please, check "IEC 62304 for Medical Device Software Development: Steps to Compliance - Webinar By GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements

Event Categories

Education: Training
Health & Medicine: Healthcare, Medical device, Pharma

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