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. 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
7.7.2 The supplier shall implement a framework that ensures robust product and process development capabilities. The process should be implemented from initial product concept and continue through the production launch phase of the project.
7.7.3 The supplier shall evaluate and mitigate quality risks utilizing FMEA or equivalent risk analysis methodology.
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:
4.1 Failure Mode and Effects Analysis (FMEA)
4.2 Process capability (PPK / CPK)
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. CM shall develop process specific Quality Plan for all Harmonic products.
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. Timeline Compaq and the Supplier will develop a basic timeline to complete the actions that are identified within this document.
Quality Planning. The SUPPLIER will carry out quality planning with the goal of safeguarding the performance specifications agreed with ZEISS, permitting a smooth start to production (first time right) and guaranteeing a reproducible production process. This planning will include both the GOODS and SERVICES provided by the SUPPLIER as well as the SUPPLIER'S bought-in parts/services and will contain structured steps for performance and process qualification. The SUPPLIER will, on its own responsibility, specify these steps and will document the individual operations and actions taken to achieve this goal. The quality planning will include the following steps as a minimum: - Conducting a feasibility study - Identification of critical/special characteristics and, as the next step, the planning and definition of design and control measures - Measures, including planning for the qualification of the product measuring/testing process and, if necessary, for the process capability - Planning and qualification of the production equipment, assembly equipment, and processes - Planning and development of testing and inspection plans including testing and inspection methods and tools - Planning and implementation of quality assessments - Definition of preventive quality measures at the premises of suppliers /subcontractors - Determination and reduction of risks in the production process by suitable methods (e.g. by an FMEA)
8.1. Feasibility study On receiving inquiries for new or modified GOODS and SERVICES, the SUPPLIER is to conduct a feasibility study with regard to technological, logistical and quality-relevant aspects (quality objectives) based on the underlying specifications including all other applicable documents. This must be submitted to ZEISS along with the offer. The feasibility study must also be conducted in the event of changes (see Change Management). Offers to ZEISS presuppose a successful outcome of the feasibility study (all requirements are met in full). In the event of a negative outcome or an outcome indicating restrictions, the matter must be reviewed with ZEISS in advance of the submission of an offer. If necessary, the form to be used for feasibility study, will be provided by ZEISS.
8.2. Critical Characteristics All performance and process characteristics specified by ZEISS must be met by the SUPPLIER. In addition to the requirements defined by ZEISS, all characteristics that are critical or special for ZEISS (hereinafter referred to as “Critical Character...
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.
