Failure Mode and Effects Analysis for Design Improvement and Design Control 2015

  • 05 Aug 2015
  • Webinar

Description

Topics
  • The wrong practices in FMEA
  • FMEA procedure-the right way
  • New paradigms for design improvement
  • Using FMEA to improve the design
  • Using FMEA for verifying design outputs
  • Using FMEA for design inputs
  • Identifying critical design features
  • Avoiding wrong practices FMEA practices for efficient results
  • FMEA for planning design validation
  • Using best strategies to mitigate risks
Who should Attend
  • Quality assurance supervisors
  • Senior managers
  • R&D engineers
  • Design engineers
  • Quality professionals
  • Production supervisors
  • Compliance professionals
  • Regulatory professionals
  • Production engineers
  • Manufacturing engineers
  • Document control specialists
  • Quality auditors

Past Events

Important

Please, check "Failure Mode and Effects Analysis for Design Improvement and Design Control" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Medical laboratories, Pharma

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