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Failure Mode and Effects Analysis: Failure Prevention in Design and Process

Catalog Area: Quality
Duration: 16 Hrs.
Modality: Online en Vivo, Presencial e In Company

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OBJECTIVE:

  • Apply the fundamentals of the AIAG & VDA FMEA Handbook (1st Edition, 2nd Printing) to prevent potential design and process failures using the structured 7-step methodology.

  • Identify functions, failure modes, effects, and causes; evaluate Severity, Occurrence, and Detection (S-O-D); determine Action Priority (AP); and define optimization actions linked to APQP, PFMEA, and Control Plan.

  • Updated to AIAG & VDA FMEA Handbook (1st Edition, 2nd Printing).

BASIC COURSE INFORMATION:

Competencies to Develop: Failure prevention, risk analysis, 7-step methodology, S-O-D/AP evaluation, cross-functional teamwork, optimization, and DFMEA-PFMEA-Control Plan traceability.

ADDRESSED TO:

Product and Process Engineering, Quality, Manufacturing, APQP/New Product Introductions, Supplier Quality, Supervisors, Managers, and personnel involved in DFMEA/PFMEA.

SYLLABUS

Module 1. AIAG & VDA FMEA Fundamentals and Evolution: Preventive purpose; key differences versus AIAG FMEA 4th Edition, and Action Priority (AP) versus traditional RPN usage.

Module 2. Step 1 – Planning and Preparation: 5Ts, scope, cross-functional team, inputs, Customer Specific Requirements (CSR), and lessons learned.

Module 3. Step 2 – Structure Analysis: Product (DFMEA) and Process (PFMEA) structure, Focus Element, and higher/lower-level elements.

Module 4. Step 3 – Function Analysis: Functions, requirements, characteristics, and performance criteria for design and process.

Module 5. Step 4 – Failure Analysis: Failure Effect (FE), Failure Mode (FM), Failure Cause (FC), and failure chain construction.

Module 6. Step 5 – Risk Analysis: S-O-D evaluation, prevention/detection controls, Action Priority (AP), special characteristics, and technical criteria.

Module 7. Step 6 – Optimization: Actions, owners, target dates, S-O-D/AP re-evaluation, effectiveness verification, and residual risk.

Module 8. Step 7 – Results Documentation and Communication: Action tracking, lessons learned, technical decisions, and FMEA updates.

Module 9. DFMEA → PFMEA → Control Plan Integration: Traceability of requirements, risks, special characteristics, and controls; link to APQP and change management.

Module 10. Practical Workshop and Assessment: Design/process case study analysis, AP determination, and definition of prevention and improvement actions.

BENEFITS

  • Prevent failures before they reach the customer.

  • Prioritize actions using Action Priority (AP).

  • Strengthen consistency across DFMEA, PFMEA, and Control Plan.

  • Reduce rejections, customer claims, and poor quality costs.

  • Improve change management and lessons learned.

  • Technical references: AIAG & VDA FMEA Handbook (1st Edition, 2nd Printing), IATF 16949:2016, AIAG APQP 3rd Edition, AIAG Control Plan 1st Edition, applicable Customer Specific Requirements (CSR).

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