Ppap production part approval process was developed by aiag the automotive industry action group and it is an important part of the comprehensive advanced product quality planning apqp approach there are five phases to apqp. Ppap data is generally submitted from a significant production run, sampled randomly. Arcelormittal usa bulk materials ppap requirements checklist. Its easytouse interface helps you to create pdf files by simply selecting the print command from any application, creating documents which can be viewed on any computer with a pdf viewer. Prior experience with the aiag ppap requirements is needed for this role, including submission levels, control plans, pfmea, process flows, cpkppk, msa and dimensional layout. Bulk suppliers are not required to provide ppaps for fiat chrysler automobiles. Organization supplier to include a copy electronic copy per regional direction. Your tolerances are automatically applied and the spec limits are calculated. A sample special customer instruction would look like this. Master sample a sample signed off by customer and supplier, that usually is used to train operators on subjective inspections such as visual or for noise. Since standard products are already in production many of the documents for ppap are not necessary. The 2digit ppap section number plus any letter if applicable, as referenced on the nexteer automotive ppap checksheet, which follows the aiag ppap manual.
A master sample is a final sample of the product that is inspected and signed off by the customer. Introduction to production part approval process ppap. Ppap production part approval process files for ford. The 1994 version of this document was created at that time, to.
Phased ppap applies to both new vehicle programs and for vehicles currently in production, i. However, this manual procedure could be very stressful and timeconsuming, while you can finish this fai tasks more easily and efficiently with our ppap fai software, qacad. The fixed cell pellet and dna will be stored in the laboratory for possible confirmation testing if an abnormality is detected on the prenatal. 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. Production part approval process ppap jesse garant. Dna will be extracted from the edta sample and used to perform maternal cell contamination testing on the maternal sample. Note the sample size, serial numbers or other method used to identifying the individual parts included in the sample. Although the process may be complex, features of a ppap report are commonly outsourced, to attain consistent part data. Ppt production part approval process ppap powerpoint. All ppap sample parts must be tagged with this label on the part and or on the box. Introduction to production part approval process ppap production part approval process ppap defines generic requirements for production part. Supplier ppap 1st issue, 2010 r retained by supplier, s submitted to danfoss if not need it, erase r or s accordingly please note.
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. Supplier production part document no cp8all47 approval. Ppap is a standardized approach that helps ensure the supplier understands all hypertherm. Supplier production part approval process ppap manual. Aug 31, 2014 a picture of the production parts is included in the ppap documentation along with the location where the parts are stored. 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 submissions and assessment. Include documentation of the parts sent as a sample product. Generally ppap levels differ only on the document submission vs retention.
Not every ppap is the same, therefore negotiation must take place before the requirement is accepted and the process put into motion. If this is not possible then we request that each element be in pdf format and not native format such as ms. Qacad is a quick, easy and lowest priced ppap production part approval process software with onetime fee for perpetual license. This part is used to train operators and give a golden sample on visual or noise for comparison purposes. This will be used to communicate back to the supplier the acceptance or rejection of the ppap. 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. While reell reserves the right to change specifications or supply chain on. Ppap team assigns the ppap submission level during the ppap request. 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.
Preparing parental blood samples for possible confirmation testing if an abnormality is detected on the prenatal array sample dna extraction of the maternal blood sample used for maternal cell contamination testing. Process description characteristic description sc outgoing customer part number supplier part number 1 of 1 dwg. Production part approval process cqmsppap metricstream supplier training version 5 user guide. This checklist identifies the documents that the customer will receive when requesting a ppap.
Ppap the guide to the production part approval process. Ppap software free download create ppap forms from pdf. A new position for lauren manufacturing the ppap coordinator is responsible for organizing, completing and maintaining ppap submissions to customers. Please deliver to quality assurance dept rev 05 april 8, 2011. This documents the warrant that the part meets the design intent. Gmna requires electronic submission of the approved and signed gm 3660 form including required attachments for proof of validation letter and the final gm 1829 with the psw ppap submission and retain in their ppap files. Balloon your part drawings and extract the characteristics in one step. This is the label to be used to identify the ppap sample part when shipped to hed. Ppap documents excel pdf format download example template. A significant production run is defined as the following. On this site you will find lots of information on building or updating a complete ppap. Ppap is a standardized approach that helps ensure the. With our free production part approval process ppap forms, you can manually complete to fill the forms on excel or other spreadsheet software. Parts submitted to production part approval process ppap must be selected from a significant production run.
Amongst other aspects they would probably be company confidential information. Copies of ppap, apqp, fmea, msa, spc, iatf guidance, isots 16949. To read pdf files, you need the adobe acrobat reader. In order to provide consistency and stability, suppliers are now required to submit a ppap report for assessment. Click on this icon to open the cooper industries ppap forms kit which is attached to this pdf manual.
All submissions must be received two weeks prior to the ppap due date. 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. This run shall be manufactured at the production site using the tooling, gaging. Please contact accurate products for more information or call us today at 773. The interval of inspection is recommended b request a change in the frequency of inspection at any time throughout the life of the part to ensure quality.
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 is a framework of requirements used in the automotive supply chain to establish confidence in suppliers and their manufacturing processes. The intent is that all data reflects the actual production process to be used during production. Oct 05, 2016 filenames for all ppap section files shall include, in this order. Please view our pdf for specific requirements for each level of ppap documentation. It is a free software installed on it is a free software installed on almost all computers automatically. 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. Production part approval process ppap is a component of. It is preferred that the ppap submission be transmitted as one 1 pdf file. Ppap documents the steps taken to develop a new product to a specification and insures the production process works. Minimum requirements for the management system of both parties are specified.
The iqs initial sample inspection report isir is an efficient computeraided software solution for the fast, simple creation and evaluation of initial sample inspection reports in both ppap, vda and customer specific formats. Document requirement to submit number of comment 1. 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. Production part approval process ppap production and part approval process ppap page 210 release. 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. The supplier is requested to supply dimensional test results for uncoated parts in the case coated parts. The production part approval process ppap is similar to a work plan or strategy. According to danfoss quality requirements the items have to be produced under normal manufacturing conditions on machines that will be used for future production. Part submission warrant psw design records authorized engineering change note documents. Phased ppap will eventually be applied globally in the production part approval process. Suppliers are required to apply the phased ppap process, including promise dates, confirmation and event completion for all new tooled parts. Measurements must be available upon customer request. Samples must be measured parts from the ppap production trial run or production run.
Pdf995 makes it easy and affordable to create professionalquality documents in the popular pdf file format. Also, a picture of any storage area and packing instructions images can be included in this section. Charges may apply for ppap andor materials testing. 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. I further affirm that these samples were produced at the production rate of hours. Remember to add a zero before singledigit section numbers. Initial sample inspection planisir iqs caq with system.
Rights and duties in view of supplied product quality are regulated. Ford motor company launched an advanced product quality planning status reporting guideline apqp fast start initiative in december 1994. A sample from the same lot of initial production run. Uf ilbii huse of a paper or email submission must have prilior approvalbh hidby the authorized sq or quality representative. Global supppp ylier quality manual ppap requirements. Sample 2 sample 3 sample 1 comment first article inspection report isir page of 1 page 1 process flow diagram supplier op. Attach this label to the outside of packaging when sending ppap sample submission to conmet. 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. Please deliver to quality assurance dept rev 05 april 8. Sampling should be taken from a representative production run, utilizing production equipment, tooling and production employees.
Created in hopes to promote a clearer understanding of the requirements. It is preferred that the ppap be 1 pdf file for the entire submission. General motors global purchasing and supply chain global. Ppap production part approval process excel templates. Supplier quality management production part approval process. 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. Sample production parts a sample from the same lot of initial production run. A sample signed off by customer and supplier, that usually is used to train operators on subjective inspections. 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. This general supplier quality agreement sqa is the basis for technical and organizational conditions and processes which are applied by the supplier and burkert in order to meet the quality goals. Ppap is part of the bigger process advanced product quality planning apqp. Also reference apqp activities and minimum submission.
The ppap package usually shows a picture of the sample and where it is kept customer or supplier. The supplier is only authorized for delivering automotive series parts to ms spaichingen hereinafter referred to as ms after the official approval of the production process and the product. The supplier should email a single pdf file consisting of the entire submission. Date legend operation inspection opins transport delay storage prepared by. Inspectionxpert helps you balloon your part drawings and create your inspection report in minutes, not hours. Free download, no registration required start qacad software free trial. Coopers expectation is that you have a designated lab internally or externally that is capable of confirming your raw material on a periodic basis. A picture of the production parts is included in the ppap documentation along with the location where the parts are stored.