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Description
PPAP is one of the most important core tools in the series, because it is the contractual submission for the part over to you from the supplier, or from you to your customer. The challenge is always in the details of such a complicated
document, and questions come up like:
In this one-day training, we answer these questions and more, both from the supplier submission side, and the perspective of the plant submitting to the customer.
This dual perspective makes the course perfect for:
Through group activities and scenario analysis, the Organizational multifunctional team, and Supplier Quality Engineers (SQE/STA) will learn how to prepare documentation applicable to the Production Part Approval Process
(PPAP) and evaluate the effectiveness of your suppliers' Advanced Product Quality Planning (APQP) by evaluating compliance with PPAP requirements
Length
1 Day (8 Hours)
Day 1
• Why Prepare and Submit PPAP
• PPAP & APQP Relationship
• What is PPAP Process - Introduction
• When Prepare and Submit PPAP - PPAP Section 1
• Where do PPAP Requirements come from?
• PPAP Process Requirements - PPAP Section 2
• Customer Notification and Submission Requirements - PPAP Section 3
• Submission to Customer - Levels of Evidence - PPAP Section 4
• Part Submission Status - PPAP Section 5
• Record Retention – PPAP Section 6
• PPAP Appendix
Plexus International brings your team together with experienced instructors in an interactive learning environment whether you are joining online or in-person. We have always believed interactivity, application, and group discussion are critical parts of an effective and sustainable learning experience. To ensure that these values hold true, and every participant can build the same caliber of knowledge, each workshop interaction includes the following functionality and features:
This course receives a certificate of completion.
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Recently APQP has moved into the 3rd edition, and with this change comes additional requirements and modifications inside of the document.
Control Plans contain the operational details that your process needs to function, in simple terms the Control Plan is the operational directions for the process.
APQP is one of the most high-level Core Tools and a guiding force for other tools like FMEA, MSA and SPC. It is important that your APQP is done correctly.
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