Approval process and advanced product quality planning projects and iaqg apqp ppap project led aiag projects for effective problem solving, cost of poor quality, supplier management and others registered vda 6. Previously, each company developed their own expectations for supplier quality systems and the corresponding assessment documents. Click on this icon to open the cooper industries ppap forms kit which is attached to this pdf manual. Production part approval process ppap ensures your suppliers understand the. Your customer will respond back and acknowledgement and may request additional change clarification or ppap submission requirements. Page 1 of 15 production part approval process ppap assessment ppap submission assessment the following general criteria and element specific are developed to drive detail for robust. Phased ppap requirements handbook nee l u m nt e n e on a f o rd. Core tools curso espanol iatf 16949 herramientas apqp, ppap. Glbl rev 02 page 1 of 55 this document contains proprietary information of johnson controls, disclosure of this publication is absolutely prohibited without the. Supplier quality management production part approval process. Core tools curso espanol iatf 16949 herramientas apqp, ppap, amef, spc y. I affirm that the samples represented by this warrent are representative of our parts, which were made by a process that meets all production part approval process manual 4th edition requirements. Supplier production part approval process ppap manual.
What is ppap, purpose of ppap, ppap documents, different. Proprietary and confidential global supplier performance standards manual 17. Service production part approval process service ppap svppap1 service production part approval process service ppap is a supplement to production. Ppap is a standardized approach that helps ensure the supplier understands all hypertherm.
Increasing costs of equipment, materials and labor. Follow supplier excellence manual dictates provide ppap submissions compliant with the latest cpsd ppap manual level 3 is default. Production part approval process ppap is a valuable tool for establishing confidence in component suppliers and their production processes. Suppliers are required to apply the phased ppap process, including promise dates, confirmation and event completion for all new tooled parts. Ppap metricstre am the interim ppap process revision 2. Effective november 1, 2008, apqp and control plan second edition replaces apqp and control plan first edition unless otherwise specified by your customer. The purpose of ppap is to determine if all of alto shaams engineering design records. An introduction to blenders window system, widgets and tools. In todays competitive manufacturing environment controlling cost and maintaining a high level of quality have become vital to a companys success. On occasion, ti automotive may be required to submit all data. Quality system requirements qs9000 was developed by the chryslerfordgeneral motors supplier quality requirements task force.
Significant production run ppap data must be submitted from a significant production run, which is identified by aiag as 300 consecutive pieces sampled randomas 300 consecutive pieces sampled randomlyly unless otherwise agreed upon by the unless otherwise agreed upon by the. Pdf aiag production part approval process ppap 4th. It is preferred that the ppap be 1 pdf file for the entire submission. Actual measurements are taken from the parts produced and are used to complete the various test sheets of ppap. Overview of the interface and functionality of all editors. Production part approval process manual and to submit ppap using the ti automotive provided checklist.
Phased ppap will eventually be applied globally in the production part approval process. This online survey tests basic competency in each of the core tools to help evaluate your current understanding of apqp ppap, fmea, msa and spc, and determine opportunities for additional training. The supplier should email a single pdf file consisting of the entire submission. Welcome to the manual for blender, the free and open source 3d creation suite. Ppap is a standardized approach that helps ensure the. 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. Supplier quality management production part approval. Understanding aiag subtier supplier management cqi19. Ppap 4th edition has been revised to be consistent with the process. I further affirm that these samples were produced at the production rate of hours.
This manual provides guidelines designed to produce a product. Production part approval process ppap production and part approval process ppap page 210 release. 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. I also certify that documented evidence of such compliance is on file and. September 2008 i gm 1927 preface this reference manual represents the collaborative efforts of multiple gm worldwide teams engaged to develop a gm common process manual that includes apqp, launch, and current quality. 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.
Phased ppap applies to both new vehicle programs and for vehicles currently in production, i. The ppap manual provides guidelines to the processes required to produce parts with consistent quality. Complete this form and email to your customer organization whenever customer notification is requiered by the ppap manual in table 3. Production part approval process ppap, 4th edition 33. Introduction to production part approval process ppap. Reference manual second edition issued june 1994, second printing february 1995 new cover only, second edition, july 2008. Production part approval process ppap is used in the automotive supply chain for establishing confidence in suppliers and their production processes. Submit ppap s on required product, parts, products or components. Measurement systems analysis reference manual daimlerchrysler, ford motor company general motors corp. This manual is intended to be comprehensive and allencompassing. If you have any questions regarding any part of this manual you are encouraged to contact your respective supplier quality engineer.
The purpose of this manual is to communicate to organizations internal and external and suppliers, common product quality planning and control plan guidelines developed jointly by chrysler, ford and general motors. Ppap may be followed for commercial parts as determined by the sde. Also, it will verify that the suppliers actual process is to plan, as documented in ppap. This reference manual was developed by a measurement systems analysis msa work group, sanctioned by the chrysler group llc, ford motor company, and general motors corporation supplier quality requirements task force, and under the auspices of the. Introduction to production part approval process ppap production part approval process ppap defines generic requirements for production part approval.
895 1328 1203 45 1266 419 1309 890 1016 896 472 1484 495 934 307 460 558 132 85 541 978 697 730 631 128 665 1116 101 525 1140 674 1142 1334 52 43 615 583 820 583 775 487 36 425 170 929 864 731 391 333 679 370