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 failure, eliminating them in the design and production planning. Ppap team assigns the ppap submission level during the ppap request. The ppap package is a series of documents which need a formal certification signoff by the supplier and approval signoff by the customer. Please contact accurate products for more information or call us today at 773. Production part approval process ppap one of the 5. Introduction to production part approval process ppap.
The documentation has to be submitted in electronically form e. Production part approval process ppap production and part approval process ppap page 410 release. Production part approval process ppap iatf 16949 core. Scribd is the worlds largest social reading and publishing site. The ppap elements give the supplier a chance to formally think through how they can handle future problems that may arise in production, and give supervisors and managers a simple road map to follow to perform their production tasks. Please view our pdf for specific requirements for each level of ppap documentation. Production part approval process ppap explained in detail.
If this is not possible then we request that each element be in pdf format and not native format such as ms. Generally ppap levels differ only on the document submission vs retention. Charges may apply for ppap andor materials testing. Production and part approval process ppap page 110.
With our free production part approval process ppap forms, you can manually complete to fill the forms on excel or other spreadsheet software. Production part approval processppap production and part approval process ppap page 410 release. You have to send 18 documents along with product sample to customer for approvals. Documentation requirements explores each of the 18 elements of the ppap documentation package. Charges may apply for ppap and or material testing. Through the ppap guideline, suppliers and customers understand the requirements to obtain part approval of supplier manufactured parts. The exact ppap requirements and documentation will vary from industry to industry. Production part approval process ppap assessment qualityone. The package represents the ppap file at submission. The customer may request a ppap at any time during the product life. Production part approval process, ppap packages, ppap definition, ppap documentation for.
If level 2 or 4 submissions shall clearly document elements being submitted. Process failure modes and effects analysis pfmea 07. Prestolite electric reserves the right to request any of these documents at any. Production part approval process ppap is a component of. Document requirement to submit number of comment 1. It is preferred that the ppap be 1 pdf file for the entire submission. The ppap bible is a manual listing suppliers requirements for ppap and the ppap documents format. The ppap production part approval process production part approval process checklist is found in the aiag ppap production part approval process manual. 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. Was proper submission level agreed upon prior to submission.
Production part approval process ppt 1 linkedin slideshare. Ppap production part approval process excel templates. Answer to faq on ppap for tdks multilayer ceramic chip capacitors mlccs. Ppap training pdf economic sectors business scribd. Pdf aiag production part approval process ppap 4th edition. Production part approval process a p p p the manuals have ppap checklists which include all requirements, called elements, for a complete ppap package.
In the event a ppap submission is not requested, cooper quality reserves the right to request any of these documents at any time during the life of the product. The design record may reference other documents making them part of the design record. Production part approval process a p p p we find the ppap requirements in a manual. Ppapmetricstre am the interim ppap process revision 2. Introduction to production part approval process ppap production part approval process ppap defines generic requirements for production part. Retentionsubmission requirements accurate products.
The purpose of ppap is to determine if all of alto shaams engineering design records. Part submission warrant psw supplier ppap worksheet cooper will require most of these and cooper specific documents. This 18 ppap production part approval process documents list are used for approvals from customers. Created in hopes to promote a clearer understanding of the requirements. The purpose of the process flow diagram is to document the steps required in the manufacturing of the. Supplier quality management production part approval. The 18 elements or documents that comprise the ppap are. There are 18 required documents which are referred to as ppap production part approval process. Production part approval process ppap defines requirements for production part approval, including production and bulk materials. A ppap is required for any new part submission as well as for approval of any change to an existing part or process. Ppap submission checklist tab 1 tab 1 warrant tab 2 tab 3 tab4 tab 5 tab 6 tab 7 tab 8 tab 8 dimensional tab 9 tab 9 material tab 10 tab 11 tab 12 tab tab 14 tab 15 tab 16 tab 17 tab 18 tab 19 tab 20 tab 20 forms and explanation tab 21. The design fmea is required if the supplier is responsible for the design of the part for example.
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. Ppap is a series of documents gathered in one specific location a binder or electronically called the ppap package. Were customer plant problems used as an aid in developing the fmea. Supplier production part approval process ppap manual. Applicable to all parts and commodities, application of these. Coopersifir i tspecific requirements tooling information form packaging form inspection plan asc only specification deviation supplierppapworksheet 1. Production part approval process ppap defines generic requirements for production part approval. Cooper quality reserves the right to request a ppap submission for a.
All process steps shall match in process flow, pfmea, control plan and must be in aiag format. Part submission warrant psw design records authorized engineering. 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. Pdf aiag production part approval process ppap 4th. Ppap is a standardized approach that helps ensure the supplier understands all hypertherm. Is there clear and proper detail provided on reason for submission. Ppap submission regardless of whether you have been asked to deliver a submission. Ppap documents in excel pdf format download free example template download free ppap forms excel file with unlocked sheets and cells. Design failure modes and effects analysis dfmea 05. On this site you will find lots of information on building or updating a complete ppap. This site includes ppap information, different level of ppap that can be requsted, examples of submissions, training providers and a checklist to make sure you your production part approval process is correct. For those in the automotive industry, there are 18 possible elements that must be checked off.
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. Below is the list of all 18 elements accompanied by a brief description for each element. A collection of all applicable ppap elements submitted to the member. 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. The checklists identify different ppap levels from 1 to 5. Is the form of dimension throughout the ppap identical in all documentation.
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