Quality and Test Planning Sample Clauses

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.
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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 (quality plan or equiva- lent) and fault prevention (P-FMEA or other equivalent failure mode, influence and criticality analy- sis). These also include the consideration of preventive measures to prevent the use of counterfeit or presumably counterfeit parts that could be delivered to the Buyer. The handling of the key characteristics of the components defined by the Buyer or the Buyer's cus- tomer must be specified and complied with by the Supplier in writing. If relevant, the key character- istics are specified in the Buyer's drawing and can be supplemented by the critical parameters from the Supplier's manufacturing process. The archiving periods for the documents belonging to the special characteristics are to be adhered to in accordance with Chapter 6.2.
Sample 1Sample 2
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 guidelines 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 & VDA FMEA Manual or the customer-specific (OEM) FMEA method. If applicable, the risks of alternative production steps must also be assessed in the process FMEA. The entire manufacturing process chain, including sub- supplier processes, must be checked for the risk potential of material mix-ups. All necessary measures are to be taken to eliminate the risk of material substitution (e.g., introduction of efficient security systems to exclude plagiarism).
Sample 1
Quality and Test Planning. Within the scope of quality and test planning, the Supplier will establish the following: − Which test characteristics are suitable for performing an appropriate test and verification of the quality level. − The measuring methods to be used and the suitability of the measuring methods for the intended measuring task. − The place and time of the quality checks to be performed. − The type and form of data collection and documentation. This includes the statistical procedure designated for quality control, such as SPC. − Response plans and responsibilities in the case of identified deviations in the quality checks. The Supplier will implement the overall concept of test planning to avoiding quality risks and to early fault detection. Test concepts designed exclusively for the detection of defective products at the end of the process do not meet Xxxxxxx'x quality requirements. The Supplier will justify the meaningfulness and expediency of the test planning to Kärcher upon request. Kärcher reserves the right to demand additional tests in the event of recognized quality risks for Kärcher.
Sample 1

Related to Quality and Test Planning

  • Quality Specifications SANMINA-SCI shall comply with the quality specifications set forth in its Quality Manual, incorporated by reference herein, a copy of which is available from SANMINA-SCI upon request.

  • Quality Assurance The parties endorse the underlying principles of the Company’s Quality Management System, which seeks to ensure that its services are provided in a manner which best conforms to the requirements of the contract with its customer. This requires the Company to establish and maintain, implement, train and continuously improve its procedures and processes, and the employees to follow the procedures, document their compliance and participate in the improvement process. In particular, this will require employees to regularly and reliably fill out documentation and checklists to signify that work has been carried out in accordance with the customer’s specific requirements. Where necessary, training will be provided in these activities.

  • Quality Assurance/Quality Control Contractor shall establish and maintain a quality assurance/quality control program which shall include procedures for continuous control of all construction and comprehensive inspection and testing of all items of Work, including any Work performed by Subcontractors, so as to ensure complete conformance to the Contract with respect to materials, workmanship, construction, finish, functional performance, and identification. The program established by Contractor shall comply with any quality assurance/quality control requirements incorporated in the Contract.

  • CONTRACT WORK HOURS AND SAFETY STANDARDS As per the Contract Work Hours and Safety Standards Act (40 U.S.C. 3701-3708), where applicable, all Customer Purchase Orders in excess of ,000 that involve the employment of mechanics or laborers must include a provision for compliance with 40 U.S.C. 3702 and 3704, as supplemented by Department of Labor regulations (29 CFR Part 5). Under 40 U.S.C. 3702 of the Act, each contractor must be required to compute the wages of every mechanic and laborer on the basis of a standard work week of 40 hours. Work in excess of the standard work week is permissible provided that the worker is compensated at a rate of not less than one and a half times the basic rate of pay for all hours worked in excess of 40 hours in the work week. The requirements of 40 U.S.C. 3704 are applicable to construction work and provide that no laborer or mechanic must be required to work in surroundings or under working conditions which are unsanitary, hazardous or dangerous. These requirements do not apply to the purchases of supplies or materials or articles ordinarily available on the open market, or contracts for transportation or transmission of intelligence.

  • Technical Specifications The Technical Specifications furnished on the CD are intended to establish the standards for quality, performance and technical requirements for all labor, workmanship, material, methods and equipment necessary to complete the Work. When specifications and drawings are provided or referenced by the County, these are to be considered part of the Scope of Work, and to be specifically documented in the Detailed Scope of Work. For convenience, the County supplied specifications, if any, and the Technical Specifications furnished on the CD.

  • Quality Standards Each Party agrees that the nature and quality of its products and services supplied in connection with the other Party's Marks will conform to quality standards set by the other Party. Each Party agrees to supply the other Party, upon request, with a reasonable number of samples of any Materials publicly disseminated by such Party which utilize the other Party's Marks. Each Party will comply with all applicable laws, regulations, and customs and obtain any required government approvals pertaining to use of the other Party's marks.

  • Quality Service Standards Price Services and the Fund may from time to time agree to certain quality service standards, as well as incentives and penalties with respect to Price Services’ Services hereunder.

  • Quality Assurance Program An employee shall be entitled to leave of absence without loss of earnings from her or his regularly scheduled working hours for the purpose of writing examinations required by the College of Nurses of Ontario arising out of the Quality Assurance Program.

  • Inspection and Testing Each Constructing Entity shall cause inspection and testing of the Interconnection Facilities that it constructs in accordance with the provisions of this section. The Construction Parties acknowledge and agree that inspection and testing of facilities may be undertaken as facilities are completed and need not await completion of all of the facilities that a Constructing Entity is building.

  • Management of Special and Technical Environment Each certificated support person demonstrates an acceptable level of performance in managing and organizing the special materials, equipment and environment essential to the specialized programs.

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