Process Certification Clause Samples
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Process Certification. In regard to Supplier's manufacturing processes, Company reserves the right to perform periodic quality surveys and evaluations including, but not limited to, analysis of manufacturing or assembly position procedures, equipment calibration, and operator performance, as well as evaluation of quality control/quality assurance and data collection and analysis procedures. Supplier shall conduct appropriate incoming inspection of components in accordance with its standard practices. Such practices may be modified from time to time to address specific conditions as requested by Company after any increases or decreases to Price resulting from such modifications have been mutually agreed upon.
Process Certification. The Supplier shall furnish Certifications of Conformance for all special processes in accordance with applicable specifications and/or engineering drawing as required by the ▇▇▇▇▇ Purchase Order. Special process certifications for serialized parts and/or assemblies must reference the applicable serial number(s) for traceability. Certifications for materials used in special processes (i.e. primer, paint, etc.) must also be included showing suppliers listed on the latest revision of the associated QPL(s). Shelf Life Items. The Supplier shall provide certifications for age sensitive materials, i.e. epoxies, paints, adhesives, etc., which reflect date of
Process Certification. SonicWALL will conduct a Process Certification Test. The purpose of this test is to verify that the Process is stable and capable of producing high quality product in volume. Required documentation will include, but not be limited to, the following. • Parts lists, schematics, and mechanical drawing(s) that have been released to manufacturing for production build. • Procedure for all phases of the production assembly and test of the Product. • Demonstration that test/burn-in times are adequate to eliminate residual infant mortality.
Process Certification. 63.1 Company has the right, subject to the terms of Article 29, to review, inspect, and evaluate Supplier’s Material and supplies, Supplier’s facilities at which Supplier manufactures Products for Company under this Agreement, including Material management systems and supply line management processes and procedures and Supplier’s sources for Material and supplies to the extent related to Supplier’s performance of its obligations under this Agreement. Company has the right to specify the types of Material used in the manufacture and/or repair of the Product and/or suppliers of Material at any time during the Term of this Agreement. If such selection of Material impacts the previously agreed to Product prices, such subsequent Product prices shall be negotiated in good faith and mutually agreed to by the parties. All changes to Material, supplies, sites of manufacture and repair, and vendors must be approved in writing by Company. In regard to Supplier’s manufacturing and repair process for the Products, Company reserves the right, subject to the terms of Article 30, to perform periodic quality audits, surveys, evaluations, and approvals, including, but not limited to, analysis of each manufacturing, assembly, and/or test position for acceptability of procedures, equipment calibration, test software including change control, and operator performance, as well as evaluation of quality control/quality assurance and data collection and analysis procedures, to the extent related to Supplier’s performance of its obligations under this Agreement.
63.2 Supplier shall conduct appropriate incoming inspection of Material used in the manufacture of Products in accordance with its standard practices and shall maintain a Supplier control, approval, and corrective action process. Such standard practices shall be subject to audit and approval by Company and Company may require Supplier to implement recommended changes in order to facilitate Supplier’s manufacture of conforming Product. Such practices may be modified from time to time to address specific conditions as requested by Company.
63.3 Subject to compliance with Article 29, Supplier agrees to provide Company reasonable access, so as not to interrupt Supplier’s production processes, to applicable test equipment at Supplier’s facilities at which Products are manufactured under this Agreement in order for Company to (a) do test program development or (b) do final prove-in or acceptance of any test programs.
Process Certification. Logitech will conduct a Process Certification Test prior to the start of Logitech Production. The purpose of this test is to have Supplier demonstrate that the Manufacturing process is stable and capable of producing high quality product in volume. Required documentation will include, but not be limited to, the following: — parts lists, schematics, and mechanical drawings that have been released to manufacturing for production build — procedures for all phases of the production assembly and test of the Products — demonstration that test/burn-in times are adequate to eliminate residual infant mortality — yield and pareto data for all tests and inspection points covering a sample quantity defined by Logitech. Pareto, as defined herein, shall mean a list of failures. At Logitech’s option, a representative of Logitech may be sent to Supplier’s factory to observe the build.
Process Certification. The Supplier shall furnish Certifications of Conformance for all special processes in accordance with applicable specifications and/or engineering drawing as required by the CUA Purchase Order. Special process certifications for serialized parts and/or assemblies must reference the applicable serial number(s) for traceability. Certifications for materials used in special processes (i.e. primer, paint, etc.) must also be included showing suppliers listed on the latest revision of the associated QPL(s).
Process Certification. Sun will conduct a Process Certification Test prior to the start of Sun Production. The purpose of this test is to have Supplier demonstrate that the Manufacturing process is stable and capable of producing high quality product in volume. Required documentation will include, but not be limited to, the following: o Parts lists, schematics. and mechanical drawings that have been released to manufacturing for production build. o Procedures for all phases of the production assembly and test of the Product. o Demonstration that test/burn-in times am adequate to eliminate residual infant mortality. o Yield and pareto data for all test and inspection points covering a sample quantity defined by Sun. Pareto, as defined herein, shall mean a list of failures. At Sun's option, a representative of Sun may be sent to Supplier's factory to observe the build.
Process Certification. SECTION 36.01. Company has the right to review, evaluate and recommend Supplier's parts and supplies and Supplier's sources for parts and supplies. If Supplier accepts Company's recommendation and this recommendation impacts previously agree-to unit prices, such prices shall be negotiated and mutually agreed to.
SECTION 36.02. In regard to Supplier's and its subcontractors manufacturing processes, and with advance notice to Supplier, Company also reserves the right to perform periodic quality surveys, evaluations and recommendations, including, but not limited to, analyses of each manufacturing or assembly position for acceptability of procedures, equipment calibration, and operator performance, as well as evaluation of quality control/quality assurance and data collection and analysis procedures.
SECTION 36.03. Supplier shall conduct appropriate incoming inspection of components in accordance with its ISO Certification standard practices. Such practices may be modified from time to time to address specific conditions as requested by Company. Such modifications and any increases or decreases to price resulting from such modifications shall be mutually agreed upon.
Process Certification
