Risk Management in Medical Devices Industry 2019

  • 2019
  • United States

Description

Topics
  • Risk Management to ISO 14971:2012
  • Introduction into Risk Management and Quality System Integration
  • Safety / Assurance case
  • Software Risk Management (IEC62304 / FDA software reviewers` guidance):
Who should Attend
  • Quality Professionals
  • Senior Quality Managers
  • Compliance Professionals
  • Regulatory Professionals
  • Design Engineers
  • Project Managers
  • Process Owners
  • Software Engineers

Past Events

Important

Please, check "Risk Management in Medical Devices Industry" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Risk Management
Health & Medicine: Medical device

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