Quality Plans. 6.1 The Supplier shall develop, within [insert number] Working Days of the Effective Date, quality plans that ensure that all aspects of the Services are the subject of quality management systems and are consistent with BS EN ISO 9001 or any equivalent standard which is generally recognised as having replaced it (“Quality Plans”).
Quality Plans. Mutually agreed upon document outlining component quality plans and assembly quality plans for Product; and
Quality Plans. The parties are committed to quality in the performance of this Agreement. Accordingly, all Products shall conform to the Purchased Material Quality Requirements set forth in Attachment B, attached hereto and incorporated by reference herein.
Quality Plans. 3.4.1 The Contractor is responsible for the proper execution of the approved quality plans. The work beyond the customer's hold points will progress only with the Owner's consent. The Owner will also undertake quality surveillance and quality audit of the Contractor's / Sub- Contractor's works, systems and procedures and quality control activities. The Contractor further agrees, that any change in the quality plan will be made only with the Owner's approval. The Contractor shall also perform all quality activities, inspection and tests agreed with the Owner to demonstrate full compliance with the contract requirements.
Quality Plans. Quality Plans shall be prepared by Seller for all areas of activity. These quality plans shall be submitted to Purchaser for review. Specific Quality Plans shall be prepared and issued as early as possible but no later than seven Days prior to the commencement of the portion of the Scope of Work which in the subject of the Plan. The format of the Quality Plans shall be agreed with Purchaser. Seller shall ensure that all activity is carried out in accordance with the Quality Plans and will notify Purchaser of any deviations as they occur. 1.4 Review Of Documents Seller shall submit for review all Quality Plans and Design Documentation as may reasonably be required by Purchaser. A schedule of drawings and documentation shall be maintained by Seller to show the current status and revision of each document. 1.5 Records Seller shall maintain records as required by the quality plans. All records including audit reports shall be made available for inspection by Purchaser, as required. Seller shall generate records in a manner coincidental with the activities to which they refer, such that the quality status of each item can be readily verified. All records shall be concisely compiled and coded. They shall, in addition be clearly cross-referenced to the parts or assemblies to which they refer. Records shall in general, be available at the time of equipment delivery. Such records shall include relevant certifications and build documentation together with any information which would facilitate the general traceability of component items or materials. All records generated during the course of performance of the Scope of Work shall be retained by Seller for a minimum period of ten years from the date of Acceptance or supplied to Purchaser for its retention. 1.6 Seller’s Responsibility Review and comment by Purchaser of the quality assurance procedures, quality plans, inspection and test arrangements operated by either Seller or his Vendors, will not relieve Seller of their obligation to provide Equipment which complies with the requirements of the Agreement. 2.0 QUALITY SURVEILLANCE 2.1 Quality Surveillance Requirements Seller shall define the items which it proposes to Vendor together with all items for which quality plans (inspection and test plans) will be submitted. Seller shall provide Purchaser's Quality Assurance Manager the name of his representative authorized as having responsibility for resolving or obtaining resolution, of any problems arising in respect ...
Quality Plans. Current quality methodologies for repeating component manufacturing and material supply management will be transferred. Both parties will work together to develop and exchange future improved quality assurance methodologies for repeating component manufacturing and supply chain management.
Quality Plans. Current quality methodologies for Module Assembly and Conditioning will be transferred as listed in Section 1. Both parties will work together to develop and exchange future improved quality assurance methodologies for Module Assembly and Conditioning. Quality information for the repeating components to be transferred will be of three categories: (1) processes that POSCO Power can duplicate to ensure the component meets the quality requirements, for example, visual inspection criteria; (2) quantitative information that FCE has measured that shows the component meets the quality requirements, for example, package and matrix dimensions; (3) certification of detailed specifications that FCE has measured but cannot transfer that ensures the component meets the quality requirements. The details of these three levels will be developed by the Joint Committee.
Quality Plans. The Parties are committed to quality in the performance of this Agreement. Accordingly, all Products shall conform to the quality assurance requirements set forth in Attachment E.
Quality Plans. The Supplier shall develop, within [insert number] Working Days of the Effective Date, quality plans that ensure that all aspects of the Services are the subject of quality management systems and are consistent with BS EN ISO 9001 or any equivalent standard which is generally recognised as having replaced it (“Quality Plans”). The Supplier shall obtain the Buyer Representative’s written approval of the Quality Plans before implementing them, which approval shall not be unreasonably withheld or delayed. The Supplier acknowledges and accepts that the Buyer's approval shall not act as an endorsement of the Quality Plans and shall not relieve the Supplier of its responsibility for ensuring that the Services are provided to the standard required by this Contract. Following the approval by the Buyer of the Quality Plans: the Supplier shall design and deliver all Deliverables in accordance with the Quality Plans; and any Changes to the Quality Plans shall be agreed in accordance with the Change Control Procedure.
Quality Plans. PPP Co.’s quality management systems will be reflected in appropriate quality plans, the standard of which will be consistent with 900001 or 900002 (as the case may be) or any equivalent standard which is generally recognised as having replaced them (or either of them) (“Quality Plans”).
