Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency 2020

  • 2020
  • United States

Description

Topics
  • How to implement the ISO 14971 framework
  • What are the current issues and recommended solutions
  • How to Use Standards to Facilitate Product-to-Market Achievements
  • Use a Traceability Report for improved risk management operations
  • Key implementation issues related to Risk Management
  • How to Use Risk Management to Identify the Critical Success Factors
  • Risk Integration Issues, especially related to the Quality System and Design Controls
  • Using Risk Management to identify key opportunities for the organization
  • Use of appropriate risk management tools beyond FMEA
Who should Attend
  • Quality Assurance
  • Product Risk Managers
  • Research & Development
  • Regulatory Affairs
  • Operations Managers
  • Project Managers
  • Engineers
  • Manufacturing Managers

Past Events

Important

Please, check "Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical device, Medical laboratories, Medical technology

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