Quality Planning. 7.7.1 The supplier shall develop the processes required for the quality planning of product. In the planning of product, the supplier shall work with Xxxxxx Scientific to: ❖ Develop quality objectives and requirements for the product ❖ Establish processes, documents, and provide resources ❖ Determine required verification, validation, monitoring, inspection and test activities and the criteria for acceptance ❖ Define records required to provide evidence of product conformity
Quality Planning. APEX PC SOLUTIONS, INC. shall be responsible for a controlled and capable process to ensure the product is in total compliance with the product specifications. ( *** )
Quality Planning. There shall be evidence of quality planning that ensures specific requirements of the PPA Documents have been identified and incorporated into the documented quality system. IFA’s requirements represent the minimum requirements. Developer shall define and document how the requirements in the PPA Documents for quality will be met. Quality planning shall be consistent with all other requirements of a Developer's quality system and shall be documented in a format to suit Developer's methods of operation. Developer shall give consideration to the following activities, as appropriate, in meeting the specified requirements for the East End Crossing:
Quality Planning. If not otherwise agreed, the supplier must apply the documents provided on the internet / supplier portal as a basis for the subsequent capability certificates. Use of own / other documents for certification require approval by MTCE and need to be agreed upon in writing. The documents can be found under the following internet address: xxxxx://xxx.xxxxxxxxxxxxxx.xx/en/supplier-portal/
Quality Planning. 5 6.2.1 Design .............................................. 5 6.2.1.1 Development ................................ 5 6.2.1.2 Prototype .................................. 5 6.2.2 Production .......................................... 6 6.2.2.1 Eval Test .................................. 6 6.2.2.2 Pilot ...................................... 6 6.2.2.3 Launch ..................................... 6 6.3 Metric Goals and Analysis .................................. 6 6.4 Training/Certifications .................................... 6
Quality Planning. Gadzoox Microsystems shall provide Compaq and must be responsible for a controlled and capable process to ensure the product is in total compliance with the product specifications.
Quality Planning. The quality of products is mainly defined in development. It is therefore necessary for the supplier to apply appropriate preventive methods of quality planning at the development stage. These measures shall include the elements described below.
Quality Planning. To ensure the product quality for all new and changed products, a quality plan according to QS 9000 APQP or VDA-Guideline is required. Main items are: ⮚ Production (machines, fixtures, tools, operational procedures, preventative maintenance). ⮚ Capacity and procurement (materials, machines, tools, fixture, test equipment, sub-contractors). ⮚ Handling, storage, preserving, packaging and dispatch. ⮚ Environmental protection during processes and the recycling of products and packaging. ⮚ Reliability analysis, product security, (producibility analysis, availabilty analysis). ⮚ Quality planning e.g. - FMEA - SPC, MFU - Control plan - Production process plan - Measuring equipment capability - Test plan, referring safety crucial features, especially DMBA (products with extra filing), S/C (significant characteristic) and C/C (critical characteristic) relevant features, - Annual requalification test
Quality Planning. 8.1 The SUPPLIER shall bear the manufacturer’s responsibility (product liability) for the contractual products and the manufacturing processes, including responsibility for the quality of the contractual products, the agreed production capacities and the subcontractors’ processes. The SUPPLIER shall take all technical and organisational measures to exclude defects and product defects. The SUPPLIER’s organisation must be such as to ensure that the contractual products and manufacturing processes (including spare parts) are in conformity with all requirements stipulated by ACPS Automotive’s customer and all statutory and official requirements as follows: • identification of the statutory and official requirements as to the safety of the contractual product and its freedom from defects; • identification of characteristics that are of relevance for the purposes of freedom from product defects; • identification of characteristics that are relevant for safety purposes in the manufacturing and production process; • communication of the aforesaid requirements throughout the SUPPLIER’s supply chain; • traceability of the contractual products throughout the manufacturing process. For this purpose, the SUPPLIER shall appoint a Product Safety & Conformity Representative (“PSCR”) in accordance with the VDA QMC, who shall be the designated contact person for, and whose name shall be supplied to, ACPS Automotive for product safety and product conformity issues. ACPS Automotive shall be notified promptly if another person is appointed to act as the SUPPLIER’s PSCR.
Quality Planning. The SUPPLIER performs a suitable quality plan with consideration to the zero defect demand and fault prevention. He uses risk assessment methods like FMEA.
