Advanced quality planning Sample Clauses

Advanced quality planning. The supplier must prepare a detailed project schedule together with BOMATEC and comply with this schedule (e.g. pursuant to VDA Volume 4 or APQP). If a schedule variance is on the horizon, BOMATEC must be notified as early as possible and the supplier must present solutions so as to still meet the deadline. The supplier is responsible for preparing appropriate QFD analyses, feasibility studies, zero- defect strategies, control plan, FMEA study including derived from this quality assurance and measurement concepts, process flow diagrams, inspection plans including test equipment and gauges, concept for equipment, resource scheduling, maintenance and packaging, as well as personnel qualification etc. The supplier undertakes to use and comply with new, competitive technologies and development planning processes, taking into account the technical conditions. It shall contribute its experience from the start of the project or development.
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Advanced quality planning. 3.1 Feasibility Commitment, Supplier Component Review (SCR) 7.2.2.2
Advanced quality planning. 3.1 Feasibility Commitment, Supplier Component Review (SCR) With each offer to Continental, the Supplier shall submit a feasibility commitment in regards to project time plan, quality targets and technical requirements. The Supplier shall perform a detailed feasibility analysis and present the outcome during a "Supplier Component Review Meeting". The main output of this meeting will be a feasibility commitment to a common agreed project time schedule, a common agreed (target) specification/drawing and a fixed supply chain.
Advanced quality planning. The Supplier must carry out systematic advanced quality planning on a rolling basis to identify all risks at an early stage so it can act to achieve series production at the desired time in the defined quality and agreed quantities. The Supplier must document the planning results as follows, including without limitation • Date and milestone plan, • Failure mode and effects analysis (FMEA), • Process plans, process layouts, QM plans for prototypes, pre-series and series, • Inspection and production plans and process instructions, • Lists of requirements for production facilities, product and process features. The date and milestone plan for joint developments between Xxxxxx and the Supplier may not be changed without Xxxxxx'x consent. The Supplier will allow Xxxxxx to see the quality planning and planning results on request at any time.
Advanced quality planning. To ensure philosophy “zero-defects quality” in all phases of the cooperation, the SUPPLIER is obligated to draw up a binding advanced quality plan for prototypes, pre-serial samples and serial production deliveries, to document this in test sequence plans (Control Plan) and to coordinate it with FREMACH. The Control Plan is in accordance with the requirements of IATF 16949, annex A. It must be agreed in advance if the advance quality planning should meet the requirements of VDA, Volume 4, Part 3, or the AIAG documents (APQP/Advanced Product Quality Planning). The commitment to “zero-defect-quality” and therewith to defect prevention as well as to continuous improvement is an essential part of SUPPLIERS obligations and valid without any exception

Related to Advanced quality planning

  • COUNTY’S QUALITY ASSURANCE PLAN The County or its agent will evaluate the Contractor’s performance under this Contract on not less than an annual basis. Such evaluation will include assessing the Contractor’s compliance with all Contract terms and conditions and performance standards. Contractor deficiencies which the County determines are severe or continuing and that may place performance of the Contract in jeopardy if not corrected will be reported to the Board of Supervisors. The report will include improvement/corrective action measures taken by the County and the Contractor. If improvement does not occur consistent with the corrective action measures, the County may terminate this Contract or impose other penalties as specified in this Contract.

  • Procurement Planning Prior to the issuance of any invitations to bid for contracts, the proposed procurement plan for the Project shall be furnished to the Association for its review and approval, in accordance with the provisions of paragraph 1 of Appendix 1 to the Guidelines. Procurement of all goods and works shall be undertaken in accordance with such procurement plan as shall have been approved by the Association, and with the provisions of said paragraph 1.

  • 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.

  • Selection Planning Prior to the issuance to consultants of any requests for proposals, the proposed plan for the selection of consultants under the Project shall be furnished to the Association for its review and approval, in accordance with the provisions of paragraph 1 of Appendix 1 to the Consultant Guidelines. Selection of all consultants’ services shall be undertaken in accordance with such selection plan as shall have been approved by the Association, and with the provisions of said paragraph 1.

  • Quality Assurance Plan The contractor shall develop and submit to NMFS a contractor Quality Assurance Plan, as referenced in Section F.5.3, which details how the contractor will ensure effectiveness and efficiency of collection efforts as well as the quality of data collected by its At-Sea Monitors. The contractor shall further establish, implement, and maintain a Quality Assurance Management program to ensure consistent quality of all work products and services performed under this contract.

  • Data Quality 4.1 Each party ensures that the shared Personal Data is accurate.

  • 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.

  • Surgery Services and Mastectomy Related Treatment This plan provides benefits for mastectomy surgery and mastectomy-related services in accordance with the Women’s Health and Cancer Rights Act of 1998 and Rhode Island General Law 27-20-29 et seq. For the member receiving mastectomy-related benefits, coverage will be provided in a manner determined in consultation with the attending physician, physician assistant, or an advance practice registered nurse and the patient, for: • all stages of reconstruction of the breast on which the mastectomy was performed; • surgery and reconstruction of the other breast to produce a symmetrical appearance; • prostheses; and • treatment of physical complications at all stages of the mastectomy, including lymphedema. See the Summary of Medical Benefits for the amount you pay.

  • Clinical Management for Behavioral Health Services (CMBHS) System The CMBHS is the official record of documentation by System Agency. Grantee shall:

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