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Quality and Test Planning Sample Clauses

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 XxxxxxxxXxxxxxxxxxx@xxxx-xxxxx.xxx).
Sample 1Sample 2See All (4)
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 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 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.

  • General specifications For the purpose of this Regulation, the vehicle shall fulfil the following requirements:

  • Evaluation, Testing, and Monitoring 1. The System Agency may review, test, evaluate and monitor Grantee’s Products and services, as well as associated documentation and technical support for compliance with the Accessibility Standards. Review, testing, evaluation and monitoring may be conducted before and after the award of a contract. Testing and monitoring may include user acceptance testing. Neither the review, testing (including acceptance testing), evaluation or monitoring of any Product or service, nor the absence of review, testing, evaluation or monitoring, will result in a waiver of the State’s right to contest the Grantee’s assertion of compliance with the Accessibility Standards. 2. Grantee agrees to cooperate fully and provide the System Agency and its representatives timely access to Products, records, and other items and information needed to conduct such review, evaluation, testing, and monitoring.

  • Prescription Safety Glasses Prescription safety glasses will be furnished by the employer. The employer retains the authority to establish reasonable rules and procedures regarding frequency of issue, replacement of damaged glasses, limits on reimbursement costs and coordination with the employer's vision plan.

Most Referenced Clauses

Most Referenced Definitions