Quality Systems definition

Quality Systems means the regulatory, manufacturing, quality control and quality assurance procedures, processes, practices, standards, instructions and any other attributes that the parties agree upon or that are otherwise required in connection with the manufacture of Materials (including, without limitation any requirements set forth in the Quality Agreement), as set forth in Exhibit D hereto (as such Exhibit may be amended by mutual agreement of Purchaser and Supplier from time to time).
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Quality Systems means a structured and planned approach to the assurance of the quality of product and services provided based upon those processes outlined in AS/NZS/ISO 9002:1994 which relate to the TGA’s code of GMP/Blood and Blood Components or any system or process relating to such an approach;
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Quality Systems means the regulatory, manufacturing, quality control and quality assurance procedures, processes, practices, standards, instructions and any other attributes that the parties agree upon or that are otherwise required in connection with DexCom Confidential the manufacture of Commercial Materials (including, without limitation any requirements set forth in the Quality Agreement), as set forth in Exhibit D hereto (as such Exhibit may be amended by mutual agreement of Purchaser and Supplier from time to time).
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Examples of Quality Systems in a sentence

  • The Contractor shall comply with the requirements for the design of Military Packaging as follows: Where there is a requirement to design UK Military or NATO Level Packaging, the work shall be undertaken by a certified organisation, or one that although non-certified is able to demonstrate that its Quality Systems and Military Package Design expertise are of an equivalent standard.

  • Seller shall maintain an objective quality program for all Goods and Services in accordance with (a) the latest revision of AGILENT's Supplier Quality Systems Requirements DWG A-5951-1665-1; and (b) any general specification set forth in this Order or otherwise supplied by AGILENT.

  • DMR: Form initiated by Quality Systems against suppliers for non-conforming raw material.

  • Quality Systems will coordinate with Purchasing, Engineering or any department deemed necessary to rectify the problem.

  • Le Fournisseur doit établir un programme qualité pour tous les Produits et Services conforme (a) à la dernière édition en vigueur des “AGILENT's Supplier Quality Systems Requirements DWG A-5951-1665-1”; et (b) à toute autre spécification mentionnée dans la Commande ou fournie par AGILENT.

  • GP shall perform all of its manufacturing obligations under this Agreement in accordance with all FDA requirements including the Quality Systems Regulations as set forth in 21 C.F.R. 820, "good laboratory practices," and "good clinical practices" to the extent applicable, and GP's own standard operating and quality control standards and applicable industry-wide standards for proper laboratory procedures and practices.

  • TheraSense will manufacture, design and --------------------------- label FreeStyle Products for the U.S. Territory in accordance with the then governing U.S. FDA Quality Systems Regulations, and for the European Territory in accordance with the then governing European Union Quality Systems Regulations.

  • This quotation and the services herein are subject to the Quality Systems Agreement between ▇▇▇▇▇▇▇▇▇-▇▇▇▇▇ and Auxilium dated December 20, 2006 and the terms and conditions contained in the Revised Quotation for Manufacture of AA4500 (Active) Registration Lots and Validation Support (Quotation 667-1-4- Revision No. 2) between ▇▇▇▇▇▇▇▇▇-▇▇▇▇▇ and Auxilium dated October 26, 2006, both of which are incorporated herein by reference.

  • All suppliers to Buyer are required to be registered to QS-9000 Quality Systems Requirements and as modified from time to time.

  • Seller, as service provider for the Products, is responsible for analysis of service reports, service repair data, service trends and telephone support for potential complaints or corrective action requirements, all as set forth in the Quality Systems Regulation and other FDA instructions.


More Definitions of Quality Systems

Quality Systems. The Seller shall implement a quality management system that is subject to Buyer review and audit. PRODUCTION METHOD CHANGES: Seller is to notify Buyer of any changes in their product and/or process, changes of suppliers and changes of manufacturing location. DISQUALIFICATION: If Seller is denied previously held quality system certification and/or has been disqualified by any of buyer’s customers, Seller shall notify Buyer of removal.
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Related to Quality Systems

  • Quality System means documented organizational procedures and policies: internal audits of those policies and procedures: management review and recommendation for quality improvement.”

  • Quality Management Plan means the portion of the Project Development Plan providing the information requested in Section 4.3 of Exhibit B to the ITP.

  • Quality Standards means the quality standards published by BSI British Standards, the National Standards Body of the United Kingdom, the International Organisation for Standardisation or other reputable or equivalent body, (and their successor bodies) that a skilled and experienced operator in the same type of industry or business sector as the Contractor would reasonably and ordinarily be expected to comply with, and as may be further detailed in the Specification.

  • Quality Management System means a set of interrelated or interacting elements that organisations use to direct and control how quality policies are implemented and quality objectives are achieved;

  • Quality Plan means the quality plan to be produced by the Contractor in accordance with Schedule S2-10 (Quality Plan);