PPAP | Production Part Approval Process Workshop with ISO/TS 16949:2009
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Production Part Approval Process (PPAP) Workshop with ISO/TS 16949:2009

Seminar Content

This one day seminar addresses the purpose of PPAP and a detailed examination of Production Part Approval Process requirements. Focuses on determining if all customer engineering, design record, and specification requirements are properly understood by the supplier, and that the production process has the potential to meet these requirements during an actual production run at the quoted production rate.

This seminar is consistent with the DCX, Ford and GM manual PPAP, 4th edition.

Who Should Attend

Program managers; design, quality, and manufacturing engineers; those who have direct responsibility for preparation, assembly or review of PPAP components or packages. Auditors and those responsible for subcontractor PPAP documentation.

Prerequisites

A general knowledge of quality systems is required.

Seminar Materials

Seminar manual and workbook.

Seminar Goals

  • Understand the requirements and timing impacts of the PPAP.
  • Provide examples and lessons learned for use in the hands-on application needed for successful PPAP submission.

Seminar Outline

  • Overview and vital general information.
  • Customer notification and submission requirements.
  • Submission levels of evidence.
  • Submission status.
  • Record retention requirements.
  • PPAP document requirements.

Course Sequence: PPAP

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