Introduction to production part approval process ppap. Records of compliance with customerspecific requirements r r s r 18. In those cases, suppliers would be required to support ti automotive with complying with this mandate. Part submission warrant psw confirmation of conformance to all print notes on psw. This lesson explores the documentation for these project management processes. Part submission warrant psw s s s s r bulk material requirements checklist for bulk material ppap only s s s s r s the supplier shall submit to the customer and retain a copy of records or documentation items. The inclusion of limited supporting data, such as some the ppap elements described in section 7.
Production part approval process cqms ppap metricstream supplier training. Charges may apply for ppap andor materials testing. Ppap submissions must be made to the challenge purchasing representative. Ppap is a standardized approach that helps ensure the. The impotant part is you go through the apqp process as dictated for a part or product. Ppap production part approval process ppa production part approval q quality. Supplier quality general procedure document no oskp2000. Approval of ppap plan supplier representative name title date customer representative name title date 14. Records of compliance with customer specific requirements 12. It is the discretion of ncr to determine when and if a ppap submission is required. Production part approval process ppap is the industry standard that ensures engineering design and product specification requirements are met. Groups aiag production part approval process ppap standard. The organization shall retain a master sample for the same period as the production part approval records, or a until a new master sample is produced for the same customer part number for customer approval, or b where a master sample is required by the design record, control plan or inspection criteria, as.
Requests for part approval must therefore be supported in official ppap format and with documented results when needed. Ppap documents excel pdf format download example template. 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. As a component of the ppap sun is registered with the international material data system imds and we maintain all materials and components for submission. Material test report a number of pictures can be included of the sample part from the same production run that has been analyzed throughout the ppap. Ppap, production part approval process, is part of the bigger process of advanced product quality planning apqp.
Supplier quality management production part approval. Oct 25, 2018 the ppap bible is a manual listing suppliers requirements for ppap and the ppap documents format. Parts tagged ppap samples 2 sample parts with every submission unless otherwise requested. The documentation has to be submitted in electronically form e. Retentionsubmission requirements accurate products. Page 4 of 15 with the design record, fmeas, control plan, work instructions and all apqp documentation. Ppt production part approval process ppap powerpoint. Well, ppap is what your customer has defined for you. According to danfoss quality requirements the items have to be produced under normal manufacturing conditions on machines that will be used for future production. A ppap is required for any new part submission as well as for approval of any change to an existing part or process. The ppap bible is a manual listing suppliers requirements for ppap and the ppap documents format. Charges may apply for ppap and or material testing.
In general, a ppap is required anytime when a new part or a change to an existing partprocess is being planned. It is a very important tool for establishing confidence in product suppliers and their production processes. As a component of the ppap sun is registered with the international material data system imds and we maintain all materials and components for submission to our customers when required. Please view our pdf for specific requirements for each level of ppap documentation. Ppap production part approval process excel templates. All ppap submission documentation should be returned via email to.
Ppap the guide to the production part approval process. Usage in other ti automotive facilities 1 year after the initial ppap shall require current status of all ppap documentation in the ppap for the additional facility. Ppap is the submission of the results runoff data, layout, sample parts, etc. Document requirement to submit number of comment 1. Ppap supplier training guide v5 page 5 of 41 cqms ppap supplier training for key processes, the right way to do the work is the only way to do the work worldwide. Is ppap the same process as a isir initial sample inspection. 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. Supplier ppap 1st issue, 2010 r retained by supplier, s submitted to danfoss if not need it, erase r or s accordingly please note. Supplier production part approval process ppap manual. Please deliver to quality assurance dept rev 05 april 8. Background apqp and ppap were initially developed by the automotive industry in the late 1980s to ensure. Case study focusing on apqpppap documentation solution. Also, a picture of any storage area and packing instructions images can be included in this section.
Sun microstamping technologies utilizes the aiag production part approval process to ensure all requirements are documented, understood, and reliably implemented. Production part approval process ppap suppliers of production parts or services must submit ppap, with sample parts and documentation for approval, per aiagppap manual guidelines. 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. Free download, no registration required start qacad software free trial. Sample production parts are sent to the customer for approval and are typically stored at either the customer or suppliers site after the product development is complete. Worlds best powerpoint templates crystalgraphics offers more powerpoint templates than anyone else in the world, with over 4 million to choose from. All ppap sample parts must be tagged with this label on the part and or on the box. Master sample a sample signed off by customer and supplier, that usually is used to train operators on subjective inspections. Ppap sample parts label pl l t d tt h thi th t id f h k i l i i f f k lift t i l 1 1.
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. Ppap is a standardized approach that helps ensure the supplier understands all hypertherm. Please deliver to quality assurance dept rev 05 april 8, 2011. The ppap package usually shows a picture of the sample and where it is kept customer or supplier. Ppap documentation must be retained per ti automotive, industry and oem customer specific requirements relating to record. Created in hopes to promote a clearer understanding of the requirements. The customer may request a ppap at any time during the product life. All ppaps shall be stored electronically so the documentation is available for all other using ti automotive facilities. The supplier will supply sample parts for ppap according the mentioned schedule also without special production order and unpaid unless ms has waived the shipment of samples formally. The main goal of cqms ppap metricstream is to drive these common processes across all business units and cummins suppliers.
Product part approval process sun microstamping technologies utilizes the aiag production part approval process to ensure all requirements are documented, understood, and reliably implemented. All submissions must be received two weeks prior to the ppap due date. The exact ppap requirements and documentation will vary from industry to industry. A sample special customer instruction would look like this. Production part approval process ppap is a component of. 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.
Enter the number or code that identifies the specific mold, cavity, andor production process used to manufacture the sample parts. 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. Master sample photo documentation of ppap parts tooling photo documentation required when manufactured with oshkosh corporation owned tooling. A faa with supporting documentation is considered to be synonymous with a level 2 ppap. Written approval must be obtained prior to making production shipment. 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. Chart and diagram slides for powerpoint beautifully designed chart and diagram s for powerpoint with visually stunning graphics and animation effects. Learn more about complex documentation processes by completing the lesson titled documentation for pmapqpppap processes. Article includes a bubbled drawing and sample parts with dimensional measurements. The supplier will supply sample parts for ppap according the mentioned schedule also without special. Sample inspection reports qualified laboratory documentation sample production parts special tools the authorized distributor does not generate any of the elements of the ppap. Learn more about complex documentation processes by completing the lesson titled documentation for pmapqp ppap processes.
Suppliers are not to ship production orders to altoshaam until notified of ppap approval 2 ppap sample parts are required for level 3 submission and are to be identified as. Jun 15, 2000 sample production parts are sent to the customer for approval and are typically stored at either the customer or suppliers site after the product development is complete. 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. A picture of the production parts is usually included in the ppap documentation along with documentation regarding the location that the parts are being stored. Process flow diagrams for families of similar parts are acceptable if. Global supppp ylier quality manual ppap requirements. Winner of the standing ovation award for best powerpoint templates from presentations magazine.
Through the ppap guideline, suppliers and customers understand the requirements to obtain part approval of supplier manufactured parts. Attach this label to the outside of packaging when sending ppap sample submission to conmet. But like the way i learned military isir, not every apqp process is the same. Applicable to all parts and commodities, application of these. Supplier quality management production part approval process. Theyll give your presentations a professional, memorable appearance the kind of sophisticated look that todays audiences expect. Please contact accurate products for more information. The responsible supplier official, after verifying that the results show conformance to all customer requirements and that all required documentation is available shall approve the declaration and provide title. Please contact accurate products for more information or call us today at 773. Supplier production part document no cp8all47 approval. Sample production parts a sample from the same lot of initial production run. Production part approval process ppap defines generic requirements for production part. The supplier is requested to supply dimensional test results for uncoated parts in the case coated parts. Our new crystalgraphics chart and diagram slides for powerpoint is a collection of over impressively designed datadriven chart and editable diagram s guaranteed to impress any audience.
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