Quality Assurance Procedure definition

Quality Assurance Procedure means Periodic Maintenance consisting of either of the following, which determines whether a device is operating accurately and properly:
Quality Assurance Procedure means Periodic Mainte- nance consisting of either of the following, which deter- mines whether a device is operating accurately and properly:

Examples of Quality Assurance Procedure in a sentence

  • Samples from the supplied batches of each item at the point of delivery/storage or distribution will be collected by the consignee as a part of Standard Quality Assurance Procedure and will be sent to QA division of OSMCL.

  • The PG binder supplier shall: • Certify that the PG binder meets NYSDOT requirements.• Include type of modification and any special handling instructions in the certification if the PG binder is modified,• Provide the design mixing and compaction temperatures on their bill of lading.• Provide AASHTO M 332 test data and all necessary shipping documents in accordance with the Department’s Materials Method 702-1 Quality Assurance Procedure for Performance-Graded (PG) Asphalt Binders.

  • The Vendor / Contractor at the time of submission of the drawings for approval from UHBVN/DHBVN is also required to submit a Quality Assurance Procedure (QAP) of the materials to be supplied for review and approval.

  • In case where the trading registration organization is a public company which has delisted under Clause 2, Article 5 of this Regulation, the reference price of the first trading day shall be the closing price or the reference price (in case the last trading day has no transaction to determine the closing price) of the last trading day in the listed market.

  • Samples from the supplied batches of each item at the point of delivery/storage or distribution will be collected by the consignee as a part of Standard Quality Assurance Procedure and will be sent to appropriate laboratory for testing.

  • The Toxicology Lab prepares and certifies two types of simulator solutions: the Quality Assurance Procedure (QAP) solutions and the External Standard solution.

  • To ensure that area sources do not have to comply with PS–17 and EPA Quality Assurance Procedure 4 when they are finalized, we determined that 40 CFR 63.8(a)(2) does not apply.

  • Hancock, G., Pearson, D., and Parsai, E.I.; Development of a Comprehensive Linac‐based Quality Assurance Procedure for a retrofitted Micro‐MLC SRS System.

  • Due Date of next calibration For more specific details on Testing Equipment Calibration, see Quality Assurance Procedure No.: QAP-3.

  • The State Toxicologist shall approve software which allows the DataMaster to meet the strict accuracy and precision standards of the Quality Assurance Procedure (QAP) and perform evidentiary breath tests in compliance with the standards required by statute and the WAC.

Related to Quality Assurance Procedure

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

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

  • 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.

  • 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;

  • Grievance Procedure is used in this Agreement, it shall be considered as including the arbitration procedure.

  • 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.

  • health and safety specification means a site, activity or project specific document prepared by the client pertaining to all health and safety requirements related to construction work;

  • Expedited review means an examination, in accordance with

  • Waste Framework Directive or “WFD” means Waste Framework Directive 2008/98/EC of the European Parliament and of the Council on waste

  • QA means quality assurance.

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

  • 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.

  • 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”).

  • 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 Agreement has the meaning set forth in Section 9.6.

  • Project Implementation Manual or “PIM” means the manual setting out the measures required for the implementation of the Project, as the same may be amended from time to time, subject to prior approval of the Association;

  • PJM Reliability Assurance Agreement means that certain Reliability Assurance Agreement Among Load Serving Entities in the PJM Region, on file with FERC as PJM Interconnection L.L.C. Rate Schedule FERC No. 44, and as amended from time to time thereafter. Schedule of Work:

  • Dispute Resolution Procedures means the procedures outlined in Annexure A of the MSA Determination.

  • Clinical nurse specialist means a registered nurse with relevant post-basic qualifications and 12 months’ experience working in the clinical area of his/her specified post-basic qualification, or a minimum of four years’ post-basic registration experience, including three years’ experience in the relevant specialist field and who satisfies the local criteria.

  • Training Plan means the plan that outlines what training and assessment will be conducted off-the-job and what will be conducted on-the-job and how the Registered Training Organisation will assist in ensuring the integrity of both aspects of the training and assessment process.

  • Designated chemical dependency specialist means a person

  • Data Protection Impact Assessment means an assessment by the Controller of the impact of the envisaged processing on the protection of Personal Data.

  • 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.

  • Dispute Resolution Procedure means the procedure for resolution of Disputes set forth in Article 26;

  • service delivery and budget implementation plan means a detailed plan approved by the executive mayor of a municipality in terms of section 53(l)(c)(ii) of the MFMA for implementing the municipality's delivery of municipal services and its annual budget, and which must indicate