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Failure Mode & Effects Analysis: Spot Errors Before Yours Customer Do

Summary

Live Webinar Recording

Recording Price: $199.00

(Includes Proprietary Materials)

Failure Modes and Effects Analysis (FMEA) is an effective quality improvement tool that identifies errors that hurt quality, and can be applied to just about any process in your organization. Your customers expect the highest quality, how can you ensure they receive it? Please join us to discover:

  • How to utilize FMEA to drive improvements and boost quality
  • Proven steps to develop your FMEA plan for your specific needs
  • Ways to build a cross-sectional team to perform your analysis
  • Real-world examples of how FMEA significantly improves quality

Program Highlights

  • FMEA: Identifying Failures that Impact Quality

    • Clearly identify failures that effect your designs & processes
    • Developing a Process or Design FMEA that eliminates potential errors
    • How to determine severity, occurrence and impact of potential failures
  • Developing a Successful Failure Modes & Effects Analysis Plan

    • Determine when to initiate FMEA: Implementation essentials to boost quality
    • Using "bottom-up" analysis to uncover the cause & evaluate a failure mode effect
    • Overcoming common barriers to FMEA preparation & prevent failures
  • Preventing Problems - Before They Happen: Protecting Your Customers

    • Driving improvements for your system's reliability, safety and maintainability
    • Calculating the Risk priority number (RPN) to solve your toughest problems
    • Practices to document actions for use in continuous quality improvements
  • Question and Answer Session - Hear expert answers to real-world FMEA questions!

About The Speaker

Angelo Scangas has extensive training experience in FMEA, internal auditing, advance product quality planning, problem solving, and project management.

  • Angelo has worked in the medical device, biomedical, automotive, and electronics industries for more than 30 years, holding positions such as director of manufacturing, director of quality, and plant manager.
  • He has assisted numerous clients in the areas of process improvement, Lean Six Sigma, ISO 9001:2008, ISO 14001, ISO/TS 16949 and ISO 13485 certifications
  • Mr. Scangas is a member of the American Society of Quality and is a certified ISO Lead Auditor.

Program Benefits

In this 60-minute audio conference, you'll learn to predict, evaluate and correct damaging failure modes to prevent errors before they reach your customers.