QC Sample definition

QC Sample shall have the meaning ascribed in Section 4.1.
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QC Sample means the quality control sample, other than regulatory samples which AGC shall retain pursuant to Section 6.7 of the General Terms and Conditions, used to perform the testing of a GMP Product.
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QC Sample shall have the meaning as set forth in Section 5.2.
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Examples of QC Sample in a sentence

  • Successful QC Sample analysis will target all analytes recovered or duplicated within these ranges.

  • Label the bottles and all copies of the paperwork as "Lab QC Sample"; the laboratory must know that this sample is for their QC analyses.

  • Fluoride QC Sample: Requirements for the fluoride QC sample are detailed in Section 7.2 of the Fluoride Analysis by Ion- Selective Electrode Method, located in Chapter 8 of this manual.

  • QC Sample containers should be checked for fluorescence before use with a 366-nm ultraviolet light source with a 6-watt bulb.

  • If the third party laboratory determines that such QC Sample meets the Release Criteria, then PCYC shall be deemed to have accepted such Batch, and shall pay for such Batch as set forth in Section 5.2. If the third party laboratory determines that such Product does not meet the Release Criteria, then such Batch shall be deemed rightfully rejected, and PCYC shall have no further obligation under this Agreement with respect to such Batch.

  • A minimum of one field sample per week or 1 per 20 samples (including field blanks and duplicates), whichever is greater, must be designated as the "Lab QC Sample" for the medium and laboratory duplicate analysis.

  • For ABC samples going to a NCDOT project, the QC Sample number is to be recorded by the Producer on the delivery ticket of the truck loaded immediately after the sample material is obtained.

  • The samples are to be numbered consecutively for the entire calendar year.For ABC samples going to an NCDOT project, the QC Sample number is to be recorded by the Producer on the delivery ticket of the truck loaded immediately after the sample material is obtained in order that a RC Sample may be taken from the corresponding area of the roadway if needed.

  • Section 4.1 describes some of the main concepts underlying the SEDD Specification, as follows: • Samples (see Section 4.1.1) • Instrument QC (see Section 4.1.2) • Method (see Section 4.1.3) • Method QC Sample (see Section 4.1.4) • Analysis (see Section 4.1.5) • Results (see Section 4.1.6) Section 4.2 provides a discussion of the more complicated analytical relationships within the SEDD Specification.

  • Their proficiency is assessed through use of a blind sample obtained from either a QC Sample Vendor or made in-house.


More Definitions of QC Sample

QC Sample shall have the meaning ascribed in Section 5.1.
Sample 1

Related to QC Sample

  • DNA sample means any material that has come from a human body and consists of or includes human cells;

  • Drug sample means a unit of a prescription drug that is not intended to be sold and is intended to promote the sale of the drug.

  • Grab sample means an individual sample collected in less than 15 minutes in conjunction with an instantaneous flow measurement.

  • API means the American Petroleum Institute.

  • Biological Samples means any physical samples obtained from Study Participants in accordance with the Protocol for the purposes of the Study.

  • Finished Product means a cannabis product in its final form to be sold at a retail premises.

  • Bulk Product means Licensed Product supplied in a form other than Finished Product which can be converted into Finished Product.

  • Samples mean representative physical examples of materials, equipment or workmanship, used to confirm compliance with requirements and/or to establish standards for use in execution of the Work.

  • MSAA Indicator Technical Specifications document means, as the context requires, either or both of the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Indicator Technical Specifications November 5, 2018 Version 1.3” and the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Target and Corridor-Setting Guidelines” as they may be amended or replaced from time to time;

  • Batch means a specific quantity of Product that is intended to be of uniform character and quality, within specified limits, and is produced during the same cycle of Manufacture as defined by the applicable Batch Record.

  • Reference biological product means the single biological product licensed pursuant to 42 U.S.C.

  • Manufactured end product means any end product in product and service codes (PSCs) 1000-9999, except—

  • Milk product or "dairy product" means cottage cheese, dry curd cottage cheese, reduced fat cottage cheese, lowfat cottage cheese, cream, light cream, light whipping cream, heavy cream, heavy whipping cream, whipped cream, whipped light cream, sour cream, acidified sour cream, cultured sour cream, half-and-half, sour half-and-half, acidified sour half-and-half, cultured sour half-and-half, reconstituted or recombined milk and milk products, concentrated milk, concentrated milk products, skim milk, lowfat milk, frozen milk concentrate, flavored milk, eggnog, buttermilk, cultured milk, cultured lowfat milk, cultured skim milk, yogurt, lowfat yogurt, nonfat yogurt, acidified milk, acidified lowfat milk, acidified skim milk, low-sodium milk, low-sodium lowfat milk, low-sodium skim milk, lactose-reduced milk, lactose-reduced lowfat milk, lactose-reduced skim milk, aseptically processed and packaged milk, milk products with added safe and suitable microbial organisms, and any other milk product made by the addition or subtraction of milkfat or addition of safe and suitable optional ingredients for protein, vitamin, or mineral fortification. Unless a product is considered a milk product under this subdivision, milk product does not include dietary products, infant formula, ice cream or other desserts, cheese, or butter. Milk products include the following:

  • Harvest batch means a specifically identified quantity of dried flower or trim, leaves, and other cannabis plant matter that is uniform in strain, harvested at the same time, and, if applicable, cultivated using the same pesticides and other agricultural chemicals, and harvested at the same time.

  • Bid sample means a sample to be furnished by a bidder to show the characteristics of the item offered in the bid.

  • Product means any deliverable under the Contract, which may include commodities, services, technology or software.

  • Produced Material means records, software and other material, whether complete or not, that, as a result of this Agreement, are produced or provided by the Contractor or a Subcontractor and includes the Incorporated Material;

  • Accelerator-produced material means any material made radioactive by a particle accelerator.

  • Aerosol coating product means a pressurized coating product containing pigments or resins that dispenses product ingredients by means of a propellant, and is packaged in a disposable can for hand-held application, or for use in specialized equipment for ground traffic/marking applications.

  • Drug Substance means an active ingredient that is intended to furnish pharmacological activity or other direct effect in the diagnosis, cure, mitigation, treatment, or prevention of disease or to affect the structure or any function of the human body, but does not include intermediates used in the synthesis of such ingredient.

  • Drug Product means a specific drug in dosage form from a known source of manufacture, whether

  • Non-Microsoft Product means any third-party-branded software, data, service, website or product, unless incorporated by Microsoft in a Product.

  • Aerosol Product means a pressurized spray system that dispenses product ingredients by means of a propellant contained in a product or a product's container, or by means of a mechanically induced force. “Aerosol Product” does not include “Pump Spray.”

  • Tobacco product manufacturer means an entity that after the date of enactment of this Act directly (and not exclusively through any affiliate):

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

  • Alternative nicotine product means any noncombustible product containing nicotine that is intended for human consumption, whether chewed, absorbed, dissolved, or ingested by any other means. "Alternative nicotine product" does not include any nicotine vapor product, tobacco product, or product regulated as a drug or device by the U.S. Food and Drug Administration (FDA) under Chapter V (21