Common use of Quality and Test Planning Clause in Contracts

Quality and Test Planning. 7.1 Feasibility Analysis/ Risk 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 in the case of the Buyer’s first order in accordance with a new or changed specification (OFWN). 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 correspond to the AIAG- or VDA method. If applicable, the risks of alternative production steps must also be assessed in the process FMEA. Handling of characteristics with special requirements for documentation and archiving (see OFWN) specified by the Buyer must be fulfilled by the Supplier (in accordance with VDA 1). These special characteristics must be supplemented by the critical parameters from the supplier's manufacturing process. All special characteristics must be taken into account in the Supplier's specification documents, e.g. in the production control or inspection plan and in the 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 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. The supplier must systematically keep and retain evaluable records of the results of quality monitoring, quality inspection and the measures taken to eliminate defects. The inspection certificate type 3.1 according to EN 10204 for the material (certificate contents see OFWN) must be made available to the customer in electronic form if possible before the actual material is delivered (e-mail box ▇▇▇▇▇▇▇▇▇▇▇▇▇▇▇▇▇▇▇@▇▇▇▇-▇▇▇▇▇.▇▇▇).

Quality and Test Planning. 7.1 Feasibility Analysis/ Analysis/Risk Analysis/ 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 or, in the case of the Buyer’s first order in accordance with from the Buyer customer, regarding the processing of a new or changed product number and with each specification change (OFWNe. 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 correspond cor- respond to the AIAG- VDA or VDA the customer-specific (OEM) FMEA method. If applicable, the risks of alternative alter- native production steps must also be assessed in the process FMEA. Handling of The special characteristics with special requirements for documentation and archiving (see OFWN) specified determined by the Buyer must be fulfilled by or the Supplier (Buyer's customer are defined in accordance with VDA 1)the Buyer's technical drawing. These special characteristics must be supplemented by the critical parameters pa- rameters from the supplier's manufacturing process. All The special characteristics must be taken into account in the drawing, in the Supplier's specification documents, e.g. in the 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 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 (OFWNsResults 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. The According to the defined test plan for the respective external service, the supplier must systematically systemati- cally keep and retain evaluable records of the results of quality process monitoring, quality inspection control and of the measures taken to eliminate defectsdefects on the basis of repeated commissioning of the external ser- vice. The inspection certificate type 3.1 according to EN 10204 for the material (certificate contents see OFWN) corresponding documents must be made available submitted to the customer in electronic form if possible before the actual material is delivered (e-mail box ▇▇▇▇▇▇▇▇▇▇▇▇▇▇▇▇▇▇▇@▇▇▇▇-▇▇▇▇▇Buyer on request.▇▇▇).