QUALITY SYSTEM AUDIT Clause Samples

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QUALITY SYSTEM AUDIT. Buyer reserves the right to audit Supplier’s facilities and records subject to the following conditions: (a) Buyer shall be entitled to conduct a full quality system audit each year unless otherwise agreed or Buyer can demonstrate that Supplier has materially breached this Agreement; (b) Buyer audits shall be conducted with reasonable advance notice and at reasonably convenient times during normal business hours; (c) all information gathered and data reviewed during any such audit shall be “Confidential Information” subject to the provisions of this Agreement; and (d) the scope of each such audit may include the systems, processes, and records related to Supplier’s performance of its obligations under this Agreement. Said audit shall not include review of Supplier’s financial records. Supplier shall cooperate with Buyer in the performance of such audit. Observations and conclusions of an audit will be issued to and promptly discussed with Supplier and corrective action shall be implemented by Supplier, at Supplier’s expense, in a timely manner, as mutually agreed; however Buyer may, in its sole discretion, accept Products from Supplier prior to Supplier’s completion of the corrective action. Buyer may visit in normal course of business as mutually agreed.
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QUALITY SYSTEM AUDIT. (a) Supplier shall maintain a compliant quality system that is subject to third party quality system audit that shall include the following elements: (i) Management Responsibility (ii) Quality System Principles (iii) Quality in Marketing (iv) Quality in Specification/Design (v) Quality in Procurement (vi) Quality in Production (vii) Control of Production (viii) Product Verification (ix) Control of Measuring and Test Equipment (x) Non-conformity (xi) Corrective Action (xii) Handling and Post-production (xiii) Quality Documentation and Records (xiv) Use of Statistical Methods (b) Such an audit shall assess the effectiveness and documentation of the various elements that comprise a functioning quality system. Supplier agrees that any deficiencies discovered in Supplier's quality system as a result of the audit(s) shall be remedied by Supplier at Supplier's expense.
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QUALITY SYSTEM AUDIT. Contractor agrees to permit Purchaser or its agent to conduct an initial and any subsequently required on-site Quality System Audits not to exceed one (1) per calendar year of the Contractor’s Quality System and to the extent possible certain subcontractors of Contractor in accordance with Exhibit C. Such evaluation shall assess the conformance to and documentation of the various elements that comprise a functioning quality system. Such elements are defined in Exhibit C. Contractor agrees to respond to any documented deficiencies within twenty (20) business days, after receipt of documented deficiencies, with a written corrective action plan detailing Contractor’s efforts to correct such deficiencies. In addition, Contractor will also allow Purchaser to review Contractor’s records of Quality System Audits it has or may perform on its own behalf on its subcontractors.
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QUALITY SYSTEM AUDIT. Supplier shall maintain a compliant quality system that is subject to third party quality system audit that shall include the following elements:
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QUALITY SYSTEM AUDIT. If requested, Supplier agrees to permit Company or its agent to conduct an initial and any subsequently required on-site quality system audit(s) (QSA) of Supplier's quality system at Company's expense. Such an audit shall assess the effectiveness and documentation of the various elements that comprise a functioning quality system which shall include, but not be limited to the following elements: GENERAL: 1. ****************************** 2. ****************************** 3 ****************************** 4. ****************************** 5. ****************************** 6. ****************************** 7. ****************************** 8. ****************************** 9. ****************************** 10. ****************************** 11. ****************************** 12. ****************************** 13. ****************************** 14. ****************************** 15. ****************************** 16. ****************************** 17. ****************************** SOFTWARE: 18. ****************************** 19. ****************************** 20. ****************************** 21. ****************************** 22. ****************************** 23. ****************************** 24. ****************************** 25. ****************************** 26. ****************************** 27. ****************************** CONFIDENTIAL MATERIAL OMITTED AND FILED SEPARATELY WITH THE COMMISION. ASTERISKS DENOTE SUCH OMISSIONS.
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QUALITY SYSTEM AUDIT. 43 6.16 ISO 9000............................................ 44 6.17 Utilization of Minority- and Women-Owned Business Enterprises. 44 6.18 Assignability............................... 45 6.19
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QUALITY SYSTEM AUDIT. 1.1 Distributor has a quality system which Supplier has reviewed Distributor shall maintain such quality system to the satisfaction of Supplier throughout the term of this Agreement. Supplier shall be entitled to conduct audits of Distributor's quality system at its cost at appropriate intervals as determined by Supplier.
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QUALITY SYSTEM AUDIT. 15.1 If requested, Supplier agrees to permit TSSL or its agent to conduct an initial and any subsequently required on-site Quality System Audit(s) (QSA) of Supplier's Quality System at TSSL's expense. Such an audit shall assess the effectiveness and documentation of the various elements that comprise a functioning quality system which may include, but not be limited to the following elements: A) Management Responsibility B) Quality System C) Contract Review D) Design Control E) Document & Data Control TSSL Proprietary Contract Number 81163-PPCG 14 March 2000 F) Purchasing G) Control of TSSL Supplied Equipment H) Equipment Identification and Traceability I) Process Control J) Inspection and Testing K) Control of Inspection, Measuring and Test Equipment L) Inspection and Test Status M) Control of Non-conforming Equipment N) Corrective Action and Preventive Action 0) Handling, Storage, Packaging, Preservation, and Delivery P) Control of Quality Records Q) Internal Quality Audits R) Training S) Servicing T)
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Related to QUALITY SYSTEM AUDIT

  • Quality Service Standards Price Services and the Fund may from time to time agree to certain quality service standards, as well as incentives and penalties with respect to Price Services’ Services hereunder.

  • Quality Management System Supplier hereby undertakes, warrants and confirms, and will ensue same for its subcontractors, to remain certified in accordance with ISO 9001 standard or equivalent. At any time during the term of this Agreement, the Supplier shall, if so instructed by ISR, provide evidence of such certifications. In any event, Supplier must notify ISR, in writing, in the event said certification is suspended and/or canceled and/or not continued.

  • Quality Standards Each Party agrees that the nature and quality of its products and services supplied in connection with the other Party's Marks will conform to quality standards set by the other Party. Each Party agrees to supply the other Party, upon request, with a reasonable number of samples of any Materials publicly disseminated by such Party which utilize the other Party's Marks. Each Party will comply with all applicable laws, regulations, and customs and obtain any required government approvals pertaining to use of the other Party's marks.

  • Quality Management Grantee will: 1. comply with quality management requirements as directed by the System Agency. 2. develop and implement a Quality Management Plan (QMP) that conforms with 25 TAC § 448.504 and make the QMP available to System Agency upon request. The QMP must be developed no later than the end of the first quarter of the Contract term. 3. update and revise the QMP each biennium or sooner, if necessary. ▇▇▇▇▇▇▇’s governing body will review and approve the initial QMP, within the first quarter of the Contract term, and each updated and revised QMP thereafter. The QMP must describe ▇▇▇▇▇▇▇’s methods to measure, assess, and improve - i. Implementation of evidence-based practices, programs and research-based approaches to service delivery; ii. Client/participant satisfaction with the services provided by ▇▇▇▇▇▇▇; iii. Service capacity and access to services; iv. Client/participant continuum of care; and v. Accuracy of data reported to the state. 4. participate in continuous quality improvement (CQI) activities as defined and scheduled by the state including, but not limited to data verification, performing self-reviews; submitting self-review results and supporting documentation for the state’s desk reviews; and participating in the state’s onsite or desk reviews. 5. submit plan of improvement or corrective action plan and supporting documentation as requested by System Agency. 6. participate in and actively pursue CQI activities that support performance and outcomes improvement. 7. respond to consultation recommendations by System Agency, which may include, but are not limited to the following: i. Staff training; ii. Self-monitoring activities guided by System Agency, including use of quality management tools to self-identify compliance issues; and iii. Monitoring of performance reports in the System Agency electronic clinical management system.

  • Quality Improvement The Parties must develop QI activities specifically for the oversight of the requirements of this MOU, including, without limitation, any applicable performance measures and QI initiatives, including those to prevent duplication of services, as well as reports that track referrals, Member engagement, and service utilization. Such QI activities must include processes to monitor the extent to which Members are able to access mental health services across SMHS and NSMHS, and Covered Service utilization. The Parties must document these QI activities in policies and procedures.