Quality control samples definition

Quality control samples means samples produced and used for the purpose of assuring quality control. Quality control samples include but are not limited to blank samples, spike samples, duplicate samples, and reference material samples.

Examples of Quality control samples in a sentence

  • The laboratory shall have quality control protocols that include the following elements:154.75(1) Quality control samples required.

  • Validation of both the field and laboratory data is undertaken prior to final acceptance and reporting of the data.• Quality control samples from both the Company and the Laboratory are assessed by the DBA and reported to the Company geologists for verification.

  • A copy of the Third Party Auditor‘s Information, Conflict of Interest, Statement of Verification, and Statement of Qualifications will be contained in Appendix C of the finalized Verification Report.

  • Quality control samples will be taken to ensure valid data are collected.

  • Quality control samples shall be analyzed within a period of time specified in the manufacturer’s quality control manual to avoid distribution of non-complying lots.

  • Quality control samples are run with each batch to validate the accuracy of the analysis.

  • Within study validation should be performed using Quality control samples in each analytical run.

  • Quality control samples obtained from sources external to the laboratory will be analyzed daily.

  • Validation of both the field and laboratory data is undertaken prior to final acceptance and reporting of the data. Quality control samples from both the Company and the Laboratory are assessed by the DBA and reported to the Company geologists for verification.

  • Quality control samples should be introduced randomly for quality assurance.

Related to Quality control samples

  • Quality control means the total of all activities performed by the Design-Builder, Designer, Construction Inspection Professional Engineering Firm and the Materials Testing Firm or Laboratory, subcontractors, producers or manufacturers to ensure that the Work performed by the Design-Builder conforms to the Contract requirements. For design, Quality Control activities shall include, but not be limited to, procedures for design quality, checking, design review including reviews for constructability, and review and approval of Working Plans. For construction, Quality Control activities shall include, but not be limited to, procedures for materials handling and construction quality, inspection, sampling and testing of materials both on site and at the plant(s), field testing of materials, obtaining and verifying Materials Certifications, record keeping, and equipment monitoring and calibration, production process control, and monitoring of environmental compliance. Quality Control also includes documentation of all QC design and construction efforts. The Scope of Work to be performed as part of the Quality Control task may be changed after the RFQ Phase.

  • air traffic control service means a service provided for the purpose of:

  • Vapor control system means a system that prevents release to the atmosphere of gasoline vapors in excess of 80 milligrams per liter of gasoline loaded (4.7 grains per liter).

  • aerodrome control service means air traffic control service for aerodrome traffic;

  • Analytical x-ray equipment means equipment used for x-ray diffraction or fluorescence analysis.

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

  • 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;

  • Analytical x-ray system means a group of components utilizing x-rays to determine the elemental composition or to examine the microstructure of materials.

  • Manufacturing Site means a location where a manufacturing

  • 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;

  • Batch means a specific quantity of Product that is intended to have uniform character and quality, within specified limits, and is produced according to a single manufacturing order during the same cycle of manufacture.

  • SOPs has the meaning set forth in Section 3.7.

  • Product Specifications means the specifications, features and/or terms of any "Contract" (as defined in the LME Rules) listed for trading on the LME, as described in the LME Rules;

  • Control system means the combination of capture and control devices used to reduce emissions to the atmosphere.

  • cGMP means current Good Manufacturing Practice as set forth in the United States Federal Food, Drug, and Cosmetic Act, as amended, and includes all rules and regulations promulgated by the FDA thereunder.

  • Manufacturing Process means any process for—

  • Traffic control signal means a device, whether manually, electrically, or mechanically operated, by which traffic is alternately directed to stop and permitted to proceed.

  • Access control means a system for allowing only approved individuals to have unescorted access to the security zone and for ensuring that all other individuals are subject to escorted access.

  • Ambient air quality standard means an established concentration, exposure time, and frequency of occurrence of air contaminant(s) in the ambient air which shall not be exceeded.

  • Technical Specifications means the detailed requirements for the Work furnished by the Architect and set forth in Book 3 of the Contract Documents.

  • technical specification means, with respect to any Software, the document setting forth the technical specifications for such Software and included in the Statement of Work.

  • Batch Record means the production record pertaining to a Batch.

  • Emission control system means the electronic engine management controller and any emission related component in the exhaust or evaporative system which supplies an input to or receives an output from this controller.

  • Product Specification means a product specification for a Medical Device set out in Schedule 2;

  • 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.

  • Inventory control system means a system described in Section 4-41a-103.