Quality Program a) The Seller shall maintain an effective quality program based upon product complexity and contractual requirements.
b) Responsibility for control of quality shall be clearly designated within the Seller’s organizational structure. The program shall provide for placement and training of inspection and other personnel who have an effect upon or are responsible for determining product and service quality. Formal certification of personnel for processes, materials, or other operations requiring special skills or training shall be maintained.
c) The Seller shall establish controls to prevent the use of non-certified materials when certified materials are required.
d) The Seller shall provide and obtain for MHD-ROCKLAND, MHD-ROCKLAND’s customers, and appropriate regulatory authorities access to any and all of its facilities, including those facilities of the Seller’s subcontractors, or any other supplier in the Seller’s supply chain where work on items is being performed or is scheduled to be performed under any Purchase Order. MHD-ROCKLAND, MHD- ROCKLAND’s customers, and appropriate regulatory bodies shall have the right to perform in-process inspection, audits, and system surveillance at the Seller’s and Seller’s subcontractors’ facilities as part of verification of conformance to the requirements of any Purchase Order at no cost to MHD- ROCKLAND.
e) In the event a component, material, part and/or product sold to MHD-ROCKLAND is found to not meet MHD-ROCKLAND requirements, in addition to noncompliance with SAE and AS5553D/AS6174A/AS6496/AS6081 standards, the Seller shall have in place verification protocols in order to enable the identification and/or recording of all nonconforming components, materials, parts and/or products in order to allow their recall and subsequent replacement, the whole at no additional cost to MHD-ROCKLAND1;
f) The Seller shall maintain complete records of all manufacturing, inspecting and testing in connection with the Items. At MHD-ROCKLAND’s election, such records shall be made available to MHD- ROCKLAND, MHD-ROCKLAND’s customers and/or appropriate regulatory agencies during the performance of any Purchase Order and for at least seven (7) years after completion of a given Purchase Order or for such longer periods, if any, as may be specified elsewhere in such Purchase Order. Upon MHD-ROCKLAND’s request, The Seller shall forward such records to MHD-ROCKLAND at no cost to MHD-ROCKLAND. The Seller shall require control of quality at ...
Quality Program. Each Party will maintain an objective quality program for all products it delivers to the other Party. Each Party's quality program will be in accordance with the current revision of HP's Supplier Quality System Requirements. Each Party will provide to the other Party a copy of its quality program and supporting test documentation.
Quality Program. Seller shall participate in Purchaser’s Quality Conformance Program, which utilizes statistical process control methods. Seller’s participation shall require the following:
(a) Seller shall furnish daily and weekly quality data directly to Purchaser.
(b) Seller shall have CSR and Stability tests performed in a manner consistent with procedures provided by Purchaser. Purchaser’s Lab will be the control Lab.
(c) Seller shall furnish Purchaser a monthly quality report in Purchaser’s designated format, an example of which is attached hereto as Schedule 4.4(c) and incorporated herein by this reference, by the tenth (10th) day of the following month. The format shall be reviewed on an annual basis.
(d) Whenever any delivery does not conform to the Coke Quality Specifications, Seller shall immediately furnish Purchaser with an off-spec report in Purchaser’s-designated format, an example of which is attached hereto as Schedule 4.4(d) and incorporated herein by this reference, defining parameter, time, cause and corrective action.
(e) Seller will report analyses of Coke to Purchaser using Purchaser’s SPP formats, examples of which are attached hereto as Schedule 4.4(e) and incorporated herein by this reference, and will modify such formats as necessary.
(f) Seller and Purchaser will exchange samples for round xxxxx testing between labs on a monthly basis.
Quality Program. In addition to Section 5, Seller shall maintain an objective quality program for all Products supplied pursuant to this Agreement. Seller shall, upon Buyer’s request, provide Buyer copies of Seller’s program and supporting test documentation. Seller shall use commercially reasonable efforts to promptly undertake, at its sole expense, all actions necessary to implement the procedures and processes to achieve the quality standards, including without limitation the processes for addressing epidemic failures. (An epidemic failure means the occurrence of failures in excess of the agreed to [AFR] allowances for Products within any three (3) month period for a period of three (3) years from the date of delivery of the products to Buyer.)
Quality Program. 5.1.1 The Contractor shall provide a Quality Program Plan (QPP)/Quality Assurance Program Plan (QAPP) in accordance with CDRL A010.
Quality Program. WISTRON agrees to apply and be bound by the quality procedures for all Products shipped pursuant to this Agreement as set forth in Exhibit F attached hereto.
Quality Program. Foundry agrees to maintain an objective quality program --------------- for all OEM Products. Foundry's program will be in accordance with quality requirements agreed to by the parties. Foundry will, upon HP's request, provide to HP copies of Foundry's program and supporting test documentation.
Quality Program. Supplier agrees to maintain an objective quality program for all OEM Products. Supplier's program will be in accordance with the current revision of Philips' Supplier Quality System Requirements, and if applicable, any additional or substitute quality requirements agreed to by the parties. Supplier will, upon Philips' request, provide to Philips' copies of Supplier's program and supporting test documentation.
Quality Program. Supplier will implement and maintain a quality program acceptable to Quest for the Goods delivered and services rendered under Quest Purchase Orders. Supplier will allow Quest to review the quality program by reviewing Supplier’s procedures, instructions, practices, processes and other related documents to determine their acceptability. Supplier will have the continuing obligation to immediately notify Quest of change or deviation from Supplier’s approved quality program and to notify Quest of any Goods delivered or services rendered during the period of such change or deviation. QUEST will at all times be entitled to place and maintain a resident quality representative at Supplier’s principal place of business or at Supplier’s subcontractor(s) to review and ensure Supplier’s performance of the approved Quality Program.
Quality Program. Supplier agrees to maintain an objective quality program for all OEM Products. Supplier’s program will be (i) in accordance with the current revision of GEMS-IT’s Supplier Quality System Requirements, (ii) consistent with regulatory requirements applicable for products of the same type as the OEM Products and for the jurisdictions where regulatory approvals for the OEM Products have been obtained, and (iii) if applicable, any additional or substitute quality requirements agreed to by the parties. Supplier will, upon GEMS-IT’s request, provide to GEMS-IT copies of Supplier’s program and supporting test documentation. Supplier shall maintain device history records for each OEM Product shipped to GEMS-IT, including the date of manufacture, identifying lot codes and serial numbers, and provide that information to GEMS-IT upon request.
