Laboratory Control Sample Sample Clauses

Laboratory Control Sample. The LCS is a sample of known composition prepared using contaminant -free water or an inert solid such as glass beads or Teflon ™ chips, which is spiked with target analytes. Each analyte in the LCS shall be spiked at a level less than or equal to the midpoint of t he calibration curve. (The midpoint is defined as the median point in the curve, not the middle of the range.) The LCS shall be carried through the complete sample preparation and analysis procedure. The LCS is used to evaluate each analytical batch and to determine whether the method is in control. Except for VOC analysis, the LCS cannot be used as the continuing calibration verification . At least one LCS shall be included in every analytical batch. If more than one LCS is analyzed in an analytical batch, results from each LCS shall be reported. A quality control failure of an analyte in one of the LCSs shall require appropriate corrective action, including re-preparation and reanalysis . Each field sample included in the batch of samples associated with the failed LCS shall be reanalyzed with a compliant LCS.
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Related to Laboratory Control Sample

  • Laboratory Testing All laboratories selected by UPS Freight for analyzing Controlled Substances Testing will be HHS certified.

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  • Quality Control Program The Contractor shall describe the Quality Control Program in a written document which shall be reviewed by the Engineer prior to the start of any production, construction, or off-site fabrication. The written Quality Control Program shall be submitted to the Engineer for review at least ten (10) calendar days before the start of construction. The Quality Control Program shall be organized to address, as a minimum, the following items:

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  • Quality Control Plan Within forty five (45) days after the design development documents are approved, the Design-Builder shall develop a quality control plan for the Project (the “Quality Control Plan”). A draft of the Quality Control Plan shall be submitted to the Department and shall be subject to the Department’s review and approval. The Quality Control Plan shall be tailored to the specific products/type of construction activities contemplated by the GMP Basis Documents, and in general, shall include a table of contents, quality control team organization, duties/responsibilities of quality control personnel, submittal procedures, inspection procedures, deficiency correction procedures, documentation process, and a list of any other specific actions or procedures that will be required for key elements of the Work.

  • Random Drug Testing All employees covered by this Agreement shall be subject to random drug testing in accordance with Appendix D.

  • Health plan specification The Employer will require health plans participating in the Group Insurance Program to develop and implement health promotion and health education programs for State employees and their dependents.

  • Quality Control A. Controlled Affiliate agrees to use the Licensed Marks and Name only in connection with the licensed services and further agrees to be bound by the conditions regarding quality control shown in attached Exhibit A as they may be amended by BCBSA from time-to-time.

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  • SHOP DRAWINGS, PRODUCT DATA AND SAMPLES 4.12.1 Shop Drawings are drawings, diagrams, schedules and other, data specially prepared for the Work by the Contractor or any Subcontractor, manufacturer, supplier or distributor to illustrate some portion of the Work.

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