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Failure Mode Effects Analysis (FMEA)

An ounce of prevention is worth a pound of cure!

Quality management system (QMS) standards include direct and indirect references to FMEA. Please refer to the following documents:

  • ISO/TS 16949:2009, Page 16, Clause 7.3: Design and development and Page 22, Sub-clause 7.5.1.1: Control plan
  • ISO 9001:2008, Page 13, Clause 5.5.3: Preventive action

FMEA can be described as a systematic group of activities intended to:

  1. recognize and evaluate the potential failure(s) of a product or a process and the effects of these failure(s) on the customer,
  2. identify actions (controls) that could eliminate or reduce the chance of the potential failure(s) from occurring, and
  3. document the entire process.

FMEA is complementary to the process of defining what a design or process must do to satisfy the customer. All FMEA's focus on design and development, whether it be of the product, or process. Effective FMEA depends on top management's commitment to the effort required in achieving customer satisfaction.

Some of the benefits of FMEA:

  • Significant design and process improvements
  • Risks analyzed and appropriate preventive actions implemented
  • Prevention of product and process nonconformities
  • Quality products realized, at the lowest possible cost, delivered on time

Jan Roovers Associates, Inc. has trained hundreds of design and process engineers as well as people in manufacturing and quality control in the development and application of Design and Process FMEA's. We encourage our course participants to bring their FMEA's to the course. Our willingness to review and discuss these FMEA's has earned us very positive feedback.

Our most requested arrangement is the 1.5-day FMEA introduction course combined with our 1-day APQP and 0.5-day PPAP courses. These courses are geared (as much as reasonably possible) towards the specific needs and expectations of the participants. Small group discussions and customized (company-specific) exercises are used to help participants internalize, and immediately apply what has been taught.

Consulting
  •  
  • FMEA (Design and Process) Methodology and Implementation
Public Courses
  •  
  • APQP-FMEA-PPAP Combination3 Days
On-site Courses
  •  
  • FMEA (Design and Process)2 Days
  •  
  • APQP-FMEA-PPAP Combination3 Days

For information about our APQP-FMEA-PPAP programs, contact us at 704.366.2926 or via e-mail info@janroovers.com.

Public Courses
in Charlotte, NC
ISO 9001:2008
Internal Auditing
  • August 30-31
  • October 11-12
  • December 13-14
  • Contact us to confirm dates
  • ISO/TS 16949:2009
    Internal Auditing
  • Contact us for dates
  • APQP-FMEA-PPAP and Control Plan Overview Course
  • Contact us for dates
  • Geometric Dimensioning & Tolerancing Course
  • Contact us for dates
  • Design of Experiments (DOE) Course
  • Contact us for dates
  • Corrective and Preventive Action Course Including Root Cause Analysis
  • Contact us for dates
  • Register soon!
    What our Clients are saying about these courses...
    "A lot of student participation"
    "Great enthusiasm from the instructor"
    "Very beneficial course for people with little or no understanding of the standard"
    "The case studies were effective in helping me understand the audit process"
    "Very interactive, interesting and informative"
    Want to register?
    Download the course flyer/registration form. Return by fax 704.365.6165 or email info@janroovers.com. Thank you for your interest.
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    Site Updated Thursday, August 19th, 2010