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Ppap manual 4th edition pdf

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Chrysler Customer-Specific Requirements for Use with PPAP, 4th Edition. 2. © Chrysler reference the bulk material section in the PPAP manual. . The supplier submits a copy of the signed/approved electronic copy (PDF) of the. AIAG PPAP Manual 4th Edition Forms (including Control Plan) Here are the links to the Aiag Fmea Manual 5th lesforgesdessalles.info - Free download Ebook, Handbook. Edition Free Pdf, Read Online Aiag Ppap Manual 4th Edition Free pdf, Free Aiag Ppap. Manual 4th Edition Free Ebook Download, Free Aiag Ppap Manual 4th.

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PPAP 4th Edition includes the following changes: e Alignment of PPA to the the text PPAP refers to the following reference manuals: Advanced Product uality. Ing. Ralf Gläßner. Production Part Approval Process 4th Edition. PPAP. Dipl.-Ing. Ralf Gläßner. . its explanation is one QS reference manual. Download as PDF, TXT or read online from Scribd . Auditing is FUN Re: Here are the Various AIAG PPAP Manual 4th Edition Forms Thank you Howard for.

Appearance Approval Report: See the Statistical Process Control reference manual. In this case, a physical sample will serve as a Master Sample. In this case the analytical record e. For bulk materials, the organization shall use the "Bulk Material Interim Approval" form, or its equivalent see Appendix F.

Mechanisms are generally described as over or under a certain threshold. These thresholds define the boundaries of the product approval and subsequent requirements for change notification. The following step provides an alternate method for assigning Occurrence ratings.

Rank Occurrence - the ranking scale in the Potential Failure ode and Effects Analysis manual difficult to relate to bulk materials and generally results in very low numbers with little differentiation the ultimate risk. The following matrix is recommended as a replacement. It evaluates the frequency occurrence based upon observed evidence the formulator has in the design.

Obtained from appropriate experimentation on the specific final product and the potential failure mode. Similar Experience: Based upon similar products or processes and the potential failure model. Based upon a clear understanding of the chemical impact of the material and the potential failure mode. Frequency ranking clarifications: High is defined as - Repeated failures Moderate is defined as - Occasional failures Low is defined as - Relatively few failures F.

Supplementing the Failure Mode Effects and Analysis manual, bulk material desig controls may also include: Variation of supplier specifications. Design controls identified by a number should be available so that the relevant content of that control cs be understood. The next step provides an alternate method for assigning Detection rankings. Rank Detection - the ranking scale in the Potential Failure Mode and Effects Analysis manual difficult to relate to bulk materials and generally results in very low numbers with little differentiation the ultimate risk.

The following matrix may be used. It evaluates the Detection as the ability of tl. Syininetric design space analyzed with appropriate statistical tools.

Screening Experiments: Screening design or ladder evaluation strategically set to develop DOE. Infonnationldata based upon similar products or processes. Potential failure mode may result in a field failure 9 ' or constitute a safety hazard or noncompliance with a government regulation High degree of customer dissatisfaction due to the nature of the failure.

May cause serious disruption to subsequent processing of the product or result in the product failing to meet its sales specifications. Will result in a customer complaint and product return. Failure causes some customer dissatisfactioii and may result in a customer complaint or limitation on shelf life.

The customer may need to make modifications or adjustments to their process to accommodate the material. The problem is liltely to be detected as part of an incoming inspection or prior to use 4. The problem will be detected during processing 5. The problem will be detected in subsequent processing steps 6. Failure causing only a slight customer annoyance. Customer will notice only a slight deterioration or inconvenience with the product or processing of the product. Reasonable to expect that the minor nature of this failure would not cause any real effect on the product or its processing by the customer.

Customer will probably not even notice the failure. Failure is almost inevitable. Additional process steps are developed to deal with the failures. I High: Similar processes have experienced repeated failures. The process is not in statistical control.

Edition 4th ppap pdf manual

Similar processes have experienced occasional failures, but not in major proportions. Similar processes have experienced isolated failures. I 2 Remote: Failure is unlikely. No failures ever associated with almost identical processes. The process is in statistical control. Absolute Certainty of Non-Detection: Controls will not or cannot detect the existence of the defect. Organization controls probably will not detect the existence of the defect, but the defect 9 may be detected by the customer.

Controls may detect the existence of the defect, but detection may not occur until packaging is underway. Controls likely to detect the existence of the failure, but not until lot acceptance testing has been completed. Tests with a higher degree of variability will have the higher ranking.

Controls have a good chance of detecting the existence of the defect before the manufacturing process has been completed. In-Process testing is used to monitor the manufacturing process. Very HigWEarly: Important raw materials are controlled via organization specifications.

UVA intended. These are not necessarily intended to be Special Characteristics. During the design phase, the Examples of manufacturing product characteristics can be process parameters control controls for final product characteristics are: This does not imply pressure, mix rate, test protocol.

During manufacture of the bullc material, process parameters are the control characteristics. During transformation from bulk Examples of customer product to final product, both bullc transformation process parameters product characteristics and final control characteristics are: Control Characteristic Mfg.

Prototype when required - A listing of tests, evaluations and their associated specificationsltolerances used to assess an experimental or developmental formulation. This may be the only control plan that is product specific. Pre-launch - Documentation of the productlprocess control characteristics, process controls affecting Special Characteristics, associated tests, and measurement systems employed during product scale up and prior to noi-mal production.

Additional items may be included at the Organization's discretion. Bulk materials often require further processing after sampling in order to make a measurement. Measurements are often destructive in nature and this prevents retesting the same sample.

Measurement variability is often imch larger for properties important in the process industries e. Standardized test methods e. MSA studies are not required where standardized tests are used, however it is still important for thc organization to understand the measurement component of variation in the test methods used.

Customer agreement on the actual requirements for MSA for either non-standard test methods or "new-to supplier" test methods should be obtained during the planning phase. Any MSA studies should be applied to each test method associated with Special Characteristics, and no to each individual product measured by the test method. Therefore, the MSA studies should be conductec as broadly as possible across all products which use a particular test method.

If the resulting variability i unacceptable, then either the studies should be conducted on a narrower class of products or action shoulc be taken to improve the test method. The manufacture of bulk materials consists of industries which span a variety of production processe: Often the production process is completed or already in place before sufficient samples can b tested. By the time the product is made again, personnel andlor equipment may have changed.

Alsc these processes have numerous input variables, many control variables, and a variety of produt variations. The effects and relationships between all thes variables and controls are also not usually known without error.

Multiple processes are usual1 interconnected, sometimes with feedback loops. There are also timing considerations and delays i reaction time. Further, measurements of component variables are generally less precise tha measurements of component parts, such that in many cases correlated variables must be used. The requirements for master sample or equivalent shall be agreed by the customer and organization. Physical Sample: Some bulk materials are stable and unchanging over an extended period of time e.

In this case, a physical sample will serve as a Master Sample. Analytical Sample Record: Other bulk materials change with time, but can be precisely quantified by appropriate analytical techniques. In this case the analytical record e. When bulk materials can not be distinctly identified or change over time, a manufacturing sample record should be generated. This record provides an "audit trail" to the information which may be stored in various documents and or electronic systems. The following is the basic information suggested to accomplish this task: The quantity of product produced.

The critical equipment required to manufacture the bulk material. Plant 1 MFG. Product Code: AB CD Control temperature of mix. Not to exceed O F. Filmformer Resin LotIBatch: AB Material Code: A Part Submission Warrant shall be prepared and submitted for approval when required by the customer. If a customer agrees that PPAP is not required, no warrant needs to be prepared.

The information required by the Submission Warrant which does not apply to bulk material e. For those organizations that have been classified as "self certifying" by a specific customer, subniission of a warrant signed only by the organization shall be evidence of PPAP approval, unless the organization is advised otherwise.

For all other organizations, evidence of PPA approval shall be a warrant signed by both the authorized customer representative and organization or other customer approval documents.

Most products will achieve approval prior to initial use. In cases where approval callnot be obtained, a "Bulk Material Interim Approval" may be granted. A form is shown on the facing page; other forins may be used.

Name assigned to Organization's manufacturing location. The Organization's designated name for the product-as identified in the Customer's Engineering Release Documents. Code DUNS number or equivalent assigned to the manufacturing location as shown on the Customer's purchase order. Customer's Part Number.

Customer Use Only. Customer Use Only Customer Representative. Submission Level that Organization is required to subinit to as defined by the Customer. Date that the Interim Approval expires.

Date organization will resubmit for production approval. Customer's Engineering Release authorizing the use of the product in the Customer's facility. Indicate reason for Interim Request. For each item marked as "17'in 15, provide explanatory details regarding problem issues and filrnish a date for problem resolution. What is being done to ensure defective product is contained, date when the action was implemented and Exit Criteria necessary to end need for continuing the action or its individual elements.

(PDF) AIAG Production Part Approval process PPAP 4th Edition | G C - lesforgesdessalles.info

Update on progress of problem resolution, generally the midpoint from issuance to expiration of the interim period. Date material is due to Customer's site. Why won't this happen again? Responsible and Authorized Organization official to ensure compliance to the above mentioned actions and dates. Product Engineer's signature, printed name, phone number, and date. Material Engineer's signature, printed name, phone number, and date.

Quality Engineer's signature, printed name, phone number, and date. Special Product Characteristics: Control Plans: Special Process Characteristics: Test Results: Process Studies: Dimensional Results: Master Sample: Measurement Systems Studies: Appearance Approval Report: Engineering Approval: Process Flow Diagram: This connection defines the interaction of specific customer plant processing steps with Special Characteristics and final product attributes of the bulk material. This interaction is especially significant when bulk materials undergo chemical or physical transfoimation s.

For bulk materials, conducting the steps outlined in this "Customer Plant Connection" is highly recommended. It is not the intent of PPAP to compromise proprietary information. This may not be applicable to all bulk materials i. It is recognized by the organization that it is their responsibility to deliver the product to the customer with the characteristics of the bulk material per organization and customer agreement.

During the transformation from bulk product to final product, both bulk product characteristics and final product attributes may be impacted by customer process controls. Since the product is frequently two products bulk and finished , there is a shared responsibility for the final product attribute. For example, percent solids and viscosity of a bulk coating which impacts the final coating's film build attribute, may be affected by the customer's mix room percent solvent reduction.

The percent reduction process parameter may therefore be controlled to aid in control of film build. The process steps at customer plants may be matrixed versus the Special Characteristics determined jointly by the organization and the customer. The Special Characteristics may then be determined, and be included in a Control Plan for the customer process.

These special control characteristic items inay be monitored and continuously improved. Assemble cross-functional teains of customer personnel for each customer process area. Include appropriate organization representatives on each team. Select Champions for each team - these are the customer process owners i. Define critical customer handling, application steps and process parameters in each area. Also review the desired final product attributes for items needing control.

From 4, develop a list of Special Characteristics and Attributes. Construct a Customer Process Matrix, using 3 as the top, and 5 as the side of a matrix. Prepare a Control Plan for each affected customer process area. Monitor and record all Special Characteristics by appropriate means control charts, checklists, etc.

Ensure stability of Special Characteristics and continuously improve where possible. Performance testing, based upon design requirements used by each OEM to select tire construction technical approval , 1-educesthe need to repeat all tests during confisrnation tests are specified by each OEM. The above definition applies to all uses of "significant production run" within PPAP. Most designs are basic to the organization's process. All additional molds shall be certified by the organization's internal certification criteria and documentation.

For tires, tooling is defined as the tire mold. This definition of tooling applies to all uses of "tooling" within PPAP. Testing is applicable only to finished tires and not to raw materials. Tire industry practice does not require chemical, physical, or metallurgical testing. Material test results are not required for PPAP. Tire uniformity force variation and balance are designated Special Characteristics. Master samples are not retained. Checking Aids see 2. AP Submission Warrant see 2.

Part Weight Mass Reference 2. The average is reported on the PSW to four 4 decimals xx. An organization supplying to subscribing truck OEMs shall comply with the requirements in this Appendix or use guidance herein for clarification of. The following additional requirements are added: The Customer has the right to request a at any time to re-qualify a production component. Feature Base Process or Past Number Generated components are qualified using the highest content configuration to qualify the master part number.

All other configurations may be approved with the submission of a PSW linking the new part number with the master past number. For bulk material and standard catalog pasts, the organization shall formally qualify their product to their design record and submit a PSW when requested by the customer.

It is important that adequate quantities of parts be manufactured during this run to confirm the quality and capability of production process at rate prior to full production. It is recognized that in low volume applications, sample sizes as small as 30 pieces may be utilized for preliminary process capability studies. When perforning the Significant Production Run, all aspects of variability within the production process should be considered and tested where practicable, e.

If projected volumes are so low that 30 samples are not attainable prior to production, interim PAP approval lnay be granted. Once the 30 consecutive production samples are produced, measured, and the quality index calculated and accepted, then the interim approval is changed to approved.

These unique numbers shall be entered onto the dimensional or test results sheet as applicable, and actual results entered onto the appropriate sheets. The organization shall also identify the print zone for each numbered characteristic as applicable. These studies could be augmented or replaced by long-term results from the same or similar process run on the same equipment with prior customer concurrence.

Master Sample see 2. Part Submission Warrant see 2. OKg, To determine part weight, the organization shall individually weigh ten randomly selected parts, and calculate and report the average weight.

At least one part shall be measured from each cavity, tool, line, or process used in product realization. Customer Notification see 3. The customer may subsequently elect to require a submission for PPAP approval. Organizations supplying to subscribing truck OEMs are required to complete the Product Process Change notification form to advise of forthcoming process or proprietary product changes. Past Name: Engineering released finished end itein part name.

Customer Part Nuinber s: Engineering released finished end itein part number. Part Revision Level: Tool Purchase Order Number: Show change level and date for submission. Additional Engineering Changes: Include all authorized engineering change documents and approval dates not yet incorporated on the drawing but which are incorporated in the past.

The design record that specifies the custoiner part number being submitted. Purchase Order Nuinber: Enter this number as found on the purchase order.

Past weight: Enter the actual weight in kilograms to four significant places. Checking Aid Number: Enter the checking aid number, if one is used for dimensional inspection, and Its Engineering Change Level and Approval Date. Organization Name and Code: Show the code assigned to the manufacturing location on the purchase order. Organization Manufacturing Address: Contact Name: Enter the name of your customer contact.

Enter the model year, vehicle name, or engine, transmission, etc. Add explanatory details in the "other" section. Identify the submission level requested by your customer.

Check the submission items if a level 4 is requested. Provide any explanatory details on the submission results; additional infomation may be attached as appropriate.

The responsible supplier official, after verifying that the results show confomance to all customer requirements and that all required documentation is available, shall approve the declaration and provide Title, Phone Number, Einail Address, and Fax Number. Leave blank. Does this part contain any restricted or reportable substances? C] Level 4 - Warrant and other requirements as defined by customer. Level 5 - Warrant with product samples and complete supporting data reviewed at supplier's manufacturing location.

Level 3 -Warrant with product samples and complete supporting data submitted to customer. Customer contact name. Customer name. Organization Part Number: The salable part number to undergo a product or process change. Engineering Revision Level: The Organization drawing revision level and date. Customer part number if applicable.

The Customer drawing revision level and date. Customer's Purchase Order number. Safety and or government regulation: Input the name and address of the company that idwill manufacture the component. Customer assigned number for organization selling the component. Customer Plant affected: List customer plants where product is used. Change Type: Check all the properties that may be affected by the change.

Design Responsibility: Check if the organization or Customer has design responsibility. Check applicable boxes for a product change. Estimate the date that the Organization will have their internal qualifications complete. Detailed Description of Change: Specific information describing the Organization's product change or process change.

Planned Implementation Date: Input the planned date to be in production with the change. Include any additional explanation or comments here. Name of person agreeing with the declaration and submitting PPCN.

Business title of the person signing the declaration. Business Phone number: Telephone number where person signing the declaration can be reached. Business Fax number: Fax number of the person signing the declaration. Email address: E-mail address of the person signing the declaration.

Date the PPCN is signed. Other required un-numbered document information should be self-explanatory. IfJrther clarijcation is necessary, please contact your customer representative.

Your customer will respond back with an acknowledgement and may request additional change clarification or PPAP submission requirements. Street Address: Planned Date of Implementation: I also certify that documented evidence of such compliance is on file and available for customer review. FAX NO: Please submit this notification at least 6 weeks prior to the planned change implementation! Contact your customer to determine if this form is available in an electronic format or if this form should be faxed.

Safety andlor government regulation: The past remains active until tooling scrap authorization is given by the appropriate customer activity. For bulk material, "active part" refers to the bulk material contracted, not the pasts that are subsequently produced from that material. Certain customers will identify appearance items on the engineering drawings. In these cases, special approval for appearance color, grain, texture, etc. After approval or interim approval, the organization is authorized to ship product as directed by the customer.

Utilizing product from an approved supplier does not relieve the organization of responsibility for the quality of that product. Examples include the presence or absence of a required label, the installation of all required fasteners. The customer's process should identify the approval authority. When this design record is used, the organization is responsible for obtaining a drawing to convey results of dimensional inspection. ILITY is the total range of inherent variation in a stable process.

They are written by organizations to address the important characteristics and engineering requirements of the product. Each part must have a Control Plan, but in many cases, "family" Control Plans can apply to a number of parts produced using a common process. It is complementary to the process of defining what a design or process must do to satisfy the customer. OOLS are drill bits, cutters, inserts, etc. SS is a set of intesselated or interacting activities which transforms inputs into outputs.

Process flow diagrams can apply to any aspect of the business. ENT is the manufacturing location within the production site which includes the production tooling, gaging, process, materials, operators, environment, and process settings, e.

Environment is defined as all of the process conditions surrounding or affecting the manufacture and quality of a part or product. Environment will vary for each site, but generally includes: ART is manufactured at the production site using the production tooling, gaging, process, materials, operators, environment, and process settings, e.

MISSION is based on specified quantities of production parts or production materials taken from the significant production sun made with production tooling, processes, and cycle times. These parts or materials submitted for production past approval are to be verified by the organization as meeting all specified requirements from the design record. TE is tlie agreed upon number of pasts produced in a planned time period to meet customer assembly or manufacturing plant production volume requirements - with consideration of other product mix and machine availability.

The agreed production rate is typically specified in the purchase agreement. Quality planning embodies the concepts of defect prevention and continual improvement as contrasted with defect detection see Advanced roduct Quality Planning and Control Plan reference manual. SAkEA - refers to the productlpast specified on the contract between the customer and organization. E is a location at which value-added manufacturing processes occur. Refer to customer-specific requirements.

For PPAP, eveiy feature of the product as identified by engineering specifications must meet requirements. Actual measurement and test results are required. Specifications should not be confused with control limits which represent "the voice of the process. See the Statistical Process Control reference manual. SUPPLIERS are providers of production materials, or production or service parts, assemblies, heat treating, welding, painting, plating or other finishing services directly to an organization supplying the OEM or other customers requiring this document.

TOOL is defined as the portion of process machinery which is specific to a component or sub-assembly. Tools or tooling are used in process machinery to transform raw material into a finished part or assembly. Examples include the diameter of a bearing journal in millimeters, the closing effort of a door in Newtons, the concentration of electrolyte in percent, or the torque of a fastener in Newton-meters.

Related Papers. By andrea salas. By Mirco Raponi. Introduction to PPAP. By Navjyot shinde. Download pdf.

Edition pdf ppap manual 4th

Thank you both very much for your quick replies! Later a GM QC guy came in and said we didn't comply with the print because of the change. Who normally works with the customer? There is no standard for who interfaces with the customer for PPAPs.

If not Ford. Good idea. Control Plan vs. I work in Medical but am an ex Automotive person from England supplying Ford. Margaret Thatcher bobdoering Re: The forms are in post 1 or just click here.

What exactly is the difference dear sir we need version-4 control plan excel format. I am extraordinarily patient provided I get my own way in the end. Nissan etc and have modified the form to suit our needs. Medical is pretty far behind in quality systems.

Inspection Plan. I am sorry but your question got overlooked some how. The "big" three: There is no actual requirement but if they are radically different they might cause eyebrows to raise. Is it only PPAP for this companies? Best regards These are the "originals" a lot of companies put there own logo instead.

Best regards Stijloor Re: Best regards No. I suggest for your own sake stick to the format and save the questions: Steav Re: Chrysler and GM originally designed these forms. Do you have a completed form as an example so that I can understand the formulas! Happy Re: Thanks a lot for any help. I do not know if there is a resseller in India but try asking them 4th November Appearance Approval Report?

Please let me know. Hi Murray. MurrayB45 1 Attachment s 13th June MicaLerm Thank you for this is verry helpful regards Mica 7th December Life and death is in the power of the tongue. I have attacehd a completed GRR so you can see how it works. All times are GMT Marc Timothy Smith. Elsmar Cove Home Page. If you have a complaint with a post in a forum discussion thread.

In accordance with Title 17 U. I also need to know about Factory assist parts.. I do not guarantee the correctness of the content. This site contains copyrighted material the use of which has not always been specifically authorized by the copyright owner. Thank you. For more information go to: We get factory assist but they may only run 3 times. They may only run as needed. Cp vs.

AIAG PPAP Manual 4th Edition Forms (Including Control Plan)

Can anyone help me with this? Catallina Re: Section In addition. Contact Marc. Elsmar Cove Archive.. Responsibility Statement: Each person is responsible for anything they post in the Elsmar Cove forum. They are not required to be PPAPed. Neither I. We believe herein constitutes a 'fair use' of any such copyrighted material as provided for in section of the US Copyright Law.

We are making such material available in our efforts to advance understanding of environmental. USA If you are having problems Registering. Activating your Registration. West Chester. Ohio Cayman Business Systems. Site courtesy of: Flag for inappropriate content. Related titles. Jump to Page. Search inside document.

The Elsmar Cove Forum http: Thanks a bunch! Azmul Fadhli. Komomondoor Varadhan. Sandeep Malik. David Sigalingging. Roberto Ugalde Resenterra. Vinay Joshi. Heera Singh. More From befoa. Ivo Mayer.