The aiag automotive industry action group has developed a variety of standard forms. The exact ppap requirements and documentation will vary from industry to industry. Please be advised if using a paper copy of this document it is uncontrolled unless otherwise identified and it is the users responsibility to verify the latest revision. Production part approval process ppap manual level 2 document. The customer may request a ppap at any time during the product life.
Ts core tools, ppap, spc, sqc, fmea, apqp, msa, control plan. Easy to use ppap forms in excel qi macros spc software for. Ppap software free download create ppap forms from pdf. Supply of sample parts and first article inspection documentation.
Ppap is a standardized approach that helps ensure the supplier understands all hypertherm. A document that shows the detailed description of the change usually called an. The documentation has to be submitted in electronically form e. Ppap production part approval process excel templates. The purpose of the part submission warrant psw is to document the. If level 2 or 4 submissions shall clearly document elements being submitted.
Please use our sample ppap form excel pdf formats to help finishing your ppap documents more efficiently. All submissions must be received two weeks prior to the ppap due date. Each sample identified and correlates to dimensional report. Introduction to production part approval process ppap production part approval process ppap defines generic requirements for production part approval. The name of the laboratory that performed the tests, part number, revision level. Ppap sample documents business process economic sectors. Submit ppaps on required product, parts, products or components. Production part approval process ppap is a component of. Pdf aiag production part approval process ppap 4th edition. Is there clear and proper detail provided on reason for submission.
Ppap documents in excel pdf format download free example template download free ppap forms excel file with unlocked sheets and cells. Production part approval process manual and to submit ppap using the ti automotive provided checklist. These requirements are fully compliant with the automotive industry action groups aiag production part approval process ppap standard revision 4 march, 2006. Requests for part approval must therefore be supported in official ppap format and with documented results when needed.
Feb 11, 2020 the production part approval process ppap is a standardized process in the automotive and aerospace industries that helps manufacturers and suppliers communicate and approve production designs and processes before, during, and after manufacture. The production part approval process ppap is a framework of requirements used in the automotive supply chain to establish confidence in suppliers and their manufacturing processes the purpose of the ppap is to ensure that the customers design has been understood by the supplier and to prove that the supplier is capable of producing parts that meet all the requirements consistently. The production part approval process ppap ensures the supplier is. The ppap process merely helps put the reporting of activities and their results into a structured and consistent format. Production part approval process ppap production and part approval process ppap page 410 release. This identifier is known as the item id, and has a format such as 2016 ppap 000029. Microsoft office applications allow saving directly to. The purpose of this document is to communicate sltn s requirements with respect to the ppap process to those companies that supply materials and components to sltn. Supplier production part approval process ppap manual. Is the form of dimension throughout the ppap identical in all documentation, metric. This demands that the supplier must maintain a quality system that develops and documents all of the requirements of a ppap submission at any time.
Follow supplier excellence manual dictates provide ppap submissions compliant with the latest cpsd ppap manual level 3 is default. The production part approval process ppap is a standardized process in the automotive and aerospace industries that helps manufacturers and suppliers communicate and approve production designs and processes before, during, and after manufacture. Fmea reflects applicable engineering change documents g n. The purpose of ppap is to determine if all of alto shaams engineering design records and specification requirements are properly understood by the supplier, and that the. Production part approval processppap production and part approval process ppap page 110 release. On occasion, ti automotive may be required to submit all data, including subcontractor ppap information using a format that complies with specific oem customer requirements. Ppap team assigns the ppap submission level during the ppap request. Document requirement to submit number of comment 1. Pdf aiag production part approval process ppap 4th. The 1994 version of this document was created at that time, to. If the supplier submits the ppap with any items in disagreement, the future corrective action must be noted in the comments column of this form and, if required, documented in an 8d included with the ppap submission. Production part approval process ppap is a component of advance product quality planning apqp developed by the automotive industry action group aiag includes fmea and control plan both as key tools of apqp and a subset of ppap apqp is an integrated system for anticipating possible modes of. Ford motor company launched an advanced product quality planning status reporting guideline apqp fast start initiative in december 1994. Supplier quality management production part approval process.
Is there a documented program for establishing sample sizes and test. Attachment can be in any readable format such as pdf, xls. Production part approval process ppap defines requirements for production part approval, including production and bulk materials. A ppap is required anytime a new part of change to an existing part or process is being planned. Qacad is a quick, easy and lowest priced ppap production part approval process software with onetime fee for perpetual license. Aiags core tools supporttm cts software was designed with industry feedback every step of the way.
Applicable to all parts and commodities, application of these. Quality system requirements qs9000 is the result of the work of a joint action group established by the us automotive manufacturers chrysler, ford and general motors. Enable protection on part tab prior to distribution. Supplier quality management production part approval. With our free production part approval process ppap forms, you can manually complete to fill the forms on excel or other spreadsheet software. Every scr, apqp and ppap including annual layout and special customer instruction has a unique identifier assigned to it. The design record may reference other documents making them part of the design record. Oct 25, 2018 the ppap bible is a manual listing suppliers requirements for ppap and the ppap documents format. The production part approval process ppap is a framework of requirements used in the automotive supply chain to establish confidence in suppliers and their manufacturing processes. Ppap requirements represent the culmination and reporting of activities that any good supplier already does. Originally developed by the american automotive industry, the ppap process defined in this manual has been tailored to hypertherms specific needs, industry and business environment. Aiag offers several documents to get you and your staff up to speed on the new iatf 16949. Ppap documents excel pdf format download example template. It tells you the year of the issue, the type of item, and a unique number.
Production part approval process ppap 4th edition secured file cannot be printed production part approval process ppap defines requirements for production part approval, including production and bulk materials. Production part approval process ppap is the industry standard that ensures engineering design and product specification requirements are met. Click on this icon to open the cooper industries ppap forms kit which is attached to this pdf manual. The supplier should email a single pdf file consisting of the entire submission. Hence it is the responsibility of the supplier to keep updating all the necessary documents at their end per level 3 requirements and ensure it is readily available for ncr upon request. Generally ppap levels differ only on the document submission vs retention. A major objective of ppap is for suppliers to provide their customers with. A sample signed off by customer and supplier, that usually is used to train. A ppap is required for any new part submission as well as for approval of any change to an existing part or process. Through the ppap guideline, suppliers and customers understand the requirements to obtain part approval of supplier manufactured parts.
The purpose of the ppap is to ensure that the customers design has been understood by the supplier and to prove that the supplier is capable of producing parts. Purchase the below documents to ensure you have all of the information you need. Production part approval process ppap assessment qualityone. Introduction to production part approval process ppap.
Ppap metricstre am the interim ppap process revision 2. Alto shaam prefers that all ppap submissions be submitted electronically via email to. You can order its production part approval process ppap manual on its website at qi macros spc addin for excel uses aiag manuals for its requirements and includes. A customer may request a ppap at any time during the life of a product. Production and part approval process ppap page 110. Free download, no registration required start qacad software free trial. The ppap process is designed to demonstrate that a supplier has developed their design and production process to meet the clients requirements, minimizing the risk of failure by effective use of apqp. Please be advised if using a paper copy of this document it is uncontrolled unless otherwise.
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