Test Samples definition

Test Samples means the specific quantity of units per Batch of Bulk Drug Product and Insertion Tools, as applicable, that are required by Regulatory Authorities in the Territory to be tested to ensure conformance of such Batch with applicable specifications for release.
Sample 1Sample 2
Test Samples has the meaning assigned in Section 2.06.
Sample 1Sample 2

Examples of Test Samples in a sentence

  • The contractor shall prepare the shipping container(s) by marking the external packages in bold letters, “Product Verification Test Samples – Do Not Post to Stock," Contract Number [ contractor insert] and Lot/Item Number [contractor insert]” adjacent to the MIL-STD-129 (latest revision) identification markings.

  • If the average aflatoxin level of Test Samples #1 and #2 is above 15 ppb, the lot fails and the laboratory shall fill out an Imported Pistachios—Failed Lot Notification report (Form FV–249).

  • Selection of Production Test Samples Not very often does a specification call for production test samples of field welding, but it does happen on occasions and therefore the inspector must have an idea of what is expected in taking these samples.

  • If the aflatoxin level of Test Sample #1 is above 10 ppb and at or below 20 ppb, the laboratory may, at the importer’s discretion, analyze Test Sample #2 and average the test results of Test Samples #1 and #2.

  • If the proper protocol was used, your measurement system may not be suitable for MPA-preserved samples; please contact us at 301- 975-3120 or jbthomas@NIST.gov.Do not analyze the test samples until you are satisfied that your system is performing properly and is suitable for the analysis of MPA-preserved serum! Protocol for Analysis of the Serum Control Materials and Test Samples The serum control material and test samples are in sealed ampoules.

  • Edwards, Statistical Analysis of ESP Verification Test Samples, WSRC- RP-94-1224, Rev.

  • If the importer directs the laboratory to proceed with the analysis of Test Sample #2, a lot will be certified as negative to aflatoxin and the laboratory shall issue an aflatoxin inspection certificate if the averaged result of Test Samples #1 and #2 is at or below 15 ppb.

  • If the importer directs the laboratory to proceed with the analysis of Test Sam- ple #2, a lot will be certified as nega- tive to aflatoxin and the laboratory shall issue an aflatoxin inspection cer- tificate if the averaged result of Test Samples #1 and #2 is at or below 15 ppb.

  • Summary of Quality Control and Contaminant Test Samples Type of SampleSample Characteristics Concentration Levels NA = not applicable, samples not fortified with any preservative, contaminant, or potential interference.

  • New Approval Applications must contain or reference the following items as described in detail in Sections 2 and 3 of this SAP.• NIOSH Standard Application Form.• Pretest Data.• Simplified Drawings.• Assembly Matrix.• Draft Approval Label(s).• Quality Assurance Manual (Manual to be submitted separately as a QA Application after first approval).• Product Quality Control Plan.o Classification of Defects Document.o Sampling Plan.• Application Fee, $200.• User Instructions.• Test Samples (Hardware).

Related to Test Samples

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

  • Manufacturing Site means a location where a manufacturing

  • 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.

  • 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.

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

  • 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.

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

  • Assay means a laboratory analysis of Crude Petroleum to include the following: A.P.I. Gravity, Reid vapor pressure, composition, pour point, water and sediment content, sulfur content, viscosity, distillation, hydrogen sulfide, flash/boiling point and other characteristics as may be required by Carrier.

  • 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 have uniform character and quality, within specified limits, and is produced according to a single manufacturing order during the same cycle of manufacture.

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

  • Finished Products means any one or more of the following petroleum oils, or a mixture or combination of these oils, to be used without further processing except blending by mechanical means:

  • Manufacturing Process means any process for—

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

  • API means American Petroleum Institute.

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

  • 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.

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

  • 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;

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

  • Recycled product means a product containing recovered material, or post-consumer recovered material, or both.

  • Harvested Material means the grain or fodder from crops of the Licensed Varieties grown from Seed or Retained Seed.

  • Output Material means any Documents or other materials, and any data or other information provided by the Supplier relating to the Specified Service;

  • Sampler means a person who is employed by or is an owner of a licensed laboratory, grower, or processor and is authorized by that employer to collect samples in accordance with the testing laboratory's standard operating procedures and these Rules.

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

  • Runtime Product means the version specific files and application program interfaces (APIs) specified in the RUNTIME.TXT file provided with SAP Crystal Reports 2008, SAP Crystal Reports for Eclipse 2.0, and SAP Crystal Reports for Visual Studio 2010.