Quality System. The CNA's quality requirements are defined in Section C, paragraph 6.0 and Section E Attachment 2, Performance Requirements Summary, of the Performance Work Statement. The CNA shall establish, maintain, and implement a Quality Control Plan (QCP) that encompasses all aspects of the agreement.
Quality System. Supplier shall maintain a documented quality system similar to the requirements set forth in the ISO 9002 standard. The intent of this quality system is to provide for business and repair processes which are repeatable, sustainable and capable of meeting Sun’s quality, cost and delivery goals.
Quality System. Suppliers of military products (AN, MS, NAS, MIL, etc) must have a quality system compliant to the applicable military quality system standard as well as the latest version of ISO 9001. Buyer reserves the right to conduct quality system audits at the Supplier facility. Supplier quality system must ensure control of product sources inclusive of but not limited to the flow down of quality requirements through the supply chain, configuration (drawing, parts list, specification, etc.) requirements, management of quality documentation, certifications, nonconformance documentation, obtaining corrective actions and performing corrective actions. Supplier quality system must ensure availability and/or retrieval upon request of quality and manufacturing records from product source.
Quality System. (a) Products will be manufactured under a quality system that ensures compliance with the Agreement and meets the required standards of the ISO 9000 and 14000 series for the Products, if applicable for SELLER.
(b) SELLER, upon written request from BUYER, will provide to BUYER copies of SELLER’s quality system documentation and supporting test documentation. At the request of BUYER, the Parties will create and maintain a combined team to provide oversight of SELLER’s quality systems to ensure SELLER’s compliance with the Agreement.
Quality System. Abbott will maintain a quality system to ensure that the Products are manufactured in accordance with: (a) applicable Quality Systems and GMP Requirements; and (b) all pertinent rules and regulations of the FDA, as the same may be amended from time to time.
Quality System. All Miltenyi Products supplied pursuant to Section 2.1 shall be manufactured and quality controlled under an appropriate quality system in accordance with Agreed Standards, as more fully described in the Quality Agreement. Any subsequent change to Miltenyi’s quality system that [***] requires the Parties to discuss and agree upon each such change in writing.
Quality System. Cordis will use its QS procedures, including, but not limited to its standard design control procedures for all Development Services and procedures for manufacturing, documentation control, purchasing control, material identification, production and process controls, inspection and measurement controls, product acceptance activities, and change control, as it pertains to the development and manufacture of the Product.
Quality System. It is the responsibility of the Supplier to provide components that conform to all current specifications provided by Thorlabs including, with respect to mechanical and optical products, the specifications and standards set forth in the Thorlabs Mechanical and Optical Standards found at xxx.xxxxxxxx.xxx under the pull tab The Company, Suppliers. Systems must be implemented to maintain specification control and testing and inspection procedures to verify product conformance. Measuring adherence to specifications shall be performed utilizing calibrated equipment traceable to NIST or equivalent standards.
Quality System. The Quality System within the Company is based on a four tier documentation system composed of the following. . Level 1, Quality Assurance Manual . Level 2, Quality Assurance Procedures (QAP's) . Level 3, Company Standards and Procedures . Xxxxx 0, Xxxxxxxxxx Standards and Database
7.1 LEVEL 1 The Quality Assurance Manual describes in outline form the Management's organization and the quality related systems in operation within the Company to meet the requirements of ISO 9001:1987. It assists the customer in making an assessment of our ability to meet the specified quality assurance requirements.
7.2 LEVEL 2 The systems outlined in the Quality Assurance Manual are enforced by separate Quality Assurance Procedures (QAP's) which describe the operational procedures of the related systems and define the responsible personnel and the objective evidence generated for substantiation. The QAP's are confidential to the Company and not for general distribution. However, at the discretion of the Company President, they may be made available for review by the customer.
Quality System. Supplier shall establish, implement and maintain throughout the Term a quality system which meets ISO-9002 and/or such other quality system as may be designated by JDSU as soon as commercially reasonable but not later than [***] months following JDSU notice to Supplier (Quality System) for the proper control of material, quality, processing, assembly, packaging and shipping of the Products. Where Supplier is certified under the foregoing and fails to obtain or maintain such certification(s), Supplier shall promptly notify JDSU. Any failure to obtain or maintain such certification(s) during the Term shall be deemed to be a breach of a material obligation in this Agreement entitling JDSU to terminate the Agreement pursuant to Section 3.3 above.
