Common use of Quality and Test Planning Clause in Contracts

Quality and Test Planning. 7.1 Feasibility Analysis/Risk Analysis/P-FMEA An analysis of the technical feasibility including the evaluation of capacity planning by the Supplier must be carried out within the scope of the enquiry or, in the case of the first order from the Buyer customer, regarding the processing of a new product number and with each specification change (e. g. new drawing index). The result of the feasibility study shall be communicated to the Buyer in writing as part of the offer documents. The Supplier shall apply adequate preventive methods of quality planning and fault prevention („Core tools“- FMEA, MSA, SPC, PPF/PPAP, APQP), if relevant. The VDA standards VDA 2, VDA 4 and VDA 5 provide a guideline. A procedure for process FMEA must be defined in writing at the Supplier's premises and must cor- respond to the VDA or the customer-specific (OEM) FMEA method. If applicable, the risks of alter- native production steps must also be assessed in the process FMEA. The special characteristics determined by the Buyer or the Buyer's customer are defined in the Buyer's technical drawing. These special characteristics must be supplemented by the critical pa- rameters from the supplier's manufacturing process. The special characteristics must be taken into account in the drawing, in the Supplier's production control or inspection plan and in the Supplier's P-FMEA. The archiving periods for the documents belonging to the special characteristics are to be adhered to in accordance with Chapter 6.2. 7.2 Production Control Plan/Inspection Planning/Documentation of Test Results 9.1). If applicable, a PCP and a test plan for the alternative production routes including alternative control and monitoring methods and work instructions must also be defined in writing. According to the defined test plan for the respective external service, the supplier must systemati- cally keep evaluable records of the results of process monitoring, quality control and of the measures taken to eliminate defects on the basis of repeated commissioning of the external ser- vice. The corresponding documents must be submitted to the Buyer on request.

Quality and Test Planning. 7.1 Feasibility Analysis/Analysis/ Risk Analysis/P-Analysis/ FMEA An analysis of the technical feasibility including the evaluation of capacity planning by the Supplier must be carried out within the scope of the enquiry or, or in the case of the Buyer’s first order from the Buyer customer, regarding the processing of in accordance with a new product number and with each or changed specification change (e. g. new drawing indexOFWN). The result of the feasibility study shall be communicated to the Buyer in writing as part of the offer documents. The Supplier shall apply adequate preventive methods of quality planning and fault prevention („Core tools“- FMEA, MSA, SPC, PPF/PPAP, APQP), if relevant. The VDA standards VDA 2, VDA 4 and VDA 5 provide a guideline. A procedure for process FMEA must be defined in writing at the Supplier's premises and must cor- respond correspond to the AIAG- or VDA or the customer-specific (OEM) FMEA method. If applicable, the risks of alter- native alternative production steps must also be assessed in the process FMEA. The Handling of characteristics with special characteristics determined requirements for documentation and archiving (see OFWN) specified by the Buyer or must be fulfilled by the Buyer's customer are defined Supplier (in the Buyer's technical drawingaccordance with VDA 1). These special characteristics must be supplemented by the critical pa- rameters parameters from the supplier's manufacturing process. The All special characteristics must be taken into account in the drawingSupplier's specification documents, e.g. in the Supplier's production control or inspection plan and in the Supplier's P-FMEA. The archiving periods for the documents belonging to the special characteristics are to be adhered to in accordance with Chapter 6.2. 7.2 Production Control Plan/Inspection Planning/Planning/ Documentation of Test Results 9.1Results Unless otherwise requested by the Buyer, the Supplier shall establish a production control plan (PCP) and an inspection plan (test criteria, test frequencies, measuring points) on its own responsibility in order to meet the agreed targets and specifications. He is responsible for testing the metal formats according to the agreed specifications (OFWNs). If applicable, a PCP and a test plan for the alternative production routes including alternative control and monitoring methods and work instructions must also be defined in writing. According to the defined test plan for the respective external service, the The supplier must systemati- cally systematically keep and retain evaluable records of the results of process quality monitoring, quality control inspection and of the measures taken to eliminate defects on the basis of repeated commissioning of the external ser- vicedefects. The corresponding documents inspection certificate type 3.1 according to EN 10204 for the material (certificate contents see OFWN) must be submitted made available to the Buyer on requestcustomer in electronic form if possible before the actual material is delivered (e-mail box XxxxxxxxXxxxxxxxxxx@xxxx-xxxxx.xxx).