Quality Audit Plans definition

Quality Audit Plans means Project Co’s audit plans defining the Internal Quality Audits and External Quality Audits that Project Co shall perform or cause to be performed on its own processes and the processes of its Principal Contractors and Subcontractors.
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Quality Audit Plans means the Concessionaire’s audit plans defining the Internal Quality Audits and External Quality Audits that the Concessionaire shall perform or cause to be performed on its own processes and the processes of its Principal Contractors and Subcontractors.
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Quality Audit Plans has the meaning given in paragraph 1 of Schedule 6 [Quality Management].
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Examples of Quality Audit Plans in a sentence

  • Project Co shall conduct Internal Quality Audits and External Quality Audits of its own processes and those of its Principal Contractors and Subcontractors (including the Designer) in accordance with the requirements of this Schedule, the Quality Documentation and the Quality Audit Plans referred to therein.

  • Project Co shall conduct Quality Audits of its own processes and those of its Sub-Contractors in accordance with the requirements of this Schedule, the Quality Documentation and the Quality Audit Plans referred to therein, provided that the Design Quality Management Plan and the Environmental Quality Management Plan shall each be subject to an initial Quality Audit within 180 days after the Effective Date.

  • There are no corresponding Quality Audit Plans as required by SOP for any Technical supplier audits for the (b)(4) contracting facility for 2012, 2013, or 2014.

  • The Mission of Residence LifeThe mission of Residence Life is to promote the mission of York College to transform lives.

  • Project Co shall submit updated Quality Audit Plans to the City’s Representative, in accordance with the Review Procedure, at 12 month intervals thereafter.

  • Project Co shall submit to the City updated Quality Audit Plans at 12 month intervals thereafter.

  • We also thank Shyam Tandon for his active participation, and discussion of the results presented here.

  • The Concessionaire will provide Quality Audit Plans that detail the Internal Quality Audits and External Quality Audits that will be conducted by the Concessionaire on its own processes and those of its contractors, subcontractors and suppliers of any tier.

  • Project Co shall submit updated Quality Audit Plans to BC Hydro’s Representative, in accordance with the Review Procedure, at 12 month intervals thereafter.

  • The public comment period was held from November 23, 2018, to Decem- ber 27, 2018, to receive input on the proposed section.


More Definitions of Quality Audit Plans

Quality Audit Plans means Project Co’s audit plans defining the Internal Quality Audits and External Quality Audits that Project Co shall perform or cause to be performed on its own processes and the processes of its Project Contractors and Sub-Contractors;
Sample 1
Quality Audit Plans means the Quality Audit Plans referred to and described in paragraph 2 of this Schedule 6.
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Related to Quality Audit Plans

  • Quality Assurance Program means the overall quality program and associated activities including the Department’s Quality Assurance, Design-Builder Quality Control, the Contract’s quality requirements for design and construction to assure compliance with Department Specifications and procedures.

  • Quality Assurance Plan or “QAP” shall have the meaning set forth in Clause 11.2;

  • Quality Assurance means a systematic procedure for assessing the effectiveness, efficiency, and appropriateness of services.

  • Project Plans mean the plans for the Project that are attached to this Agreement as Exhibit “B.”

  • Development Plans means a coherent set of operations defined and financed exclusively by the OCTs in the framework of their own policies and strategies of development, and those agreed upon between an OCT and the Member State to which it is linked;

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

  • Non-Participating Certified Clinical Nurse Specialist means a Certified Clinical Nurse Specialist who does not have a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Participating Certified Clinical Nurse Specialist means a Certified Clinical Nurse Specialist who has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • 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 Surveillance Engineer / Inspector means any person appointed by or on behalf of the Purchaser to inspect or carry out quality surveillance on supplies, stores or work under the Contract or any person deputed by the Quality Surveillance Engineer for the said purpose.

  • Diagnostic clinical procedures manual means a collection of written procedures that describes each method (and other instructions and precautions) by which the licensee performs diagnostic clinical procedures; where each diagnostic clinical procedure has been approved by the authorized user and includes the radiopharmaceutical, dosage, and route of administration.

  • Independent educational evaluation means an evaluation conducted by a qualified examiner who is not employed by the public agency responsible for the education of the child in question.

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

  • Peer-reviewed medical literature means a scientific study published only after having been critically

  • Benchmark Review means a review of the Services carried out in accordance with paragraphs 2.1 to 2.3 of Schedule 7 (Value for Money) of this Framework Agreement to determine whether those Services represent Good Value;

  • Architectural Review Committee or “ARC” shall mean the architectural review committee established by the Organization to review plans submitted to the Organization for architectural review.

  • Utilization review plan or "plan" means a written procedure for performing review.

  • Quality Manager means the individual identified by the Design-Builder who is responsible for the overall Quality Control program and Quality Control activities of the Design-Builder, including the quality of management, design and construction. (also referred to as the “Quality Control Manager”).

  • Commercialization Plan has the meaning set forth in Section 6.2.

  • Development Plan has the meaning set forth in Section 3.2.

  • 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.

  • Clinical review criteria means the written screening procedures, decision abstracts, clinical protocols, and practice guidelines used by a health carrier to determine the necessity and appropriateness of health care services.

  • Architectural Control Committee means and refer to that committee constituted under Article 4 hereof for the review of Development Plans (as hereinafter defined) and other functions.

  • Radiopharmaceutical quality assurance means, but is not limited to, the performance of appropriate chemical, biological, and physical tests on potential radiopharmaceuticals and the interpretation of the resulting data to determine their suitability for use in humans and animals, including internal test assessment, authentication of product history, and the keeping of proper records.

  • Clinical evaluation means a systematic and planned process to continuously generate, collect, analyse and assess the clinical data pertaining to a device in order to verify the safety and performance, including clinical benefits, of the device when used as intended by the manufacturer;

  • Independent testing laboratory means an independent organization, accepted by the Contracting Officer, engaged to perform specific inspections or tests of the work, either at the site or elsewhere, and report the results of these inspections or tests.