Product Testing definition

Product Testing means the design and development of preclinical or clinical test or study protocols, assays and/or measurement tools or methods, and the conduct of preclinical and clinical testing and/or validation activities, in each case relating to devices.
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Product Testing means testing of any food product (raw materials, ingredients, in-process foods, or finished products)
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Examples of Product Testing in a sentence

  • Following are the components of the Product Testing and Certification Service provided by XXXX.

  • To ensure a consistent means for measuring the power consumption of electronics products, the following protocol must be followed, which has three main components: Product Testing Set-up and Conditions: Outlined below in Sections 1(a) through (h) are the ambient test conditions and measurement protocols that must be respected when performing power measurements.

  • Supplier shall bear the costs of all such Product Testing and shall reimburse Indus for all such costs as incurred, provided that to the extent there shall be amounts due to Supplier under the Payment Settlement provisions below, such amounts due from Supplier for Product Testing may be set off against amounts then due to Supplier from Indus.

  • Product Testing Set-up, Methodology, and Documentation: The testing and measurement methods below reference published specifications from the Video Electronics Standards Association (VESA) Display Metrology Committee and the International Electrotechnical Commission (IEC), and supplement those guidelines where necessary with methods developed in cooperation with the computer monitor industry.

  • Product Testing Protocol Target Organisms • XXXX (including specific tests E.

  • To the extent that any Products fail Product Testing (“Defective Products”), Indus shall promptly notify Supplier in writing.

  • Indus will also provide Supplier with detailed cost reports for Product Testing and other reimbursable costs incurred by the fifth day of the following month, and such costs will be subtracted from the Net Sales Proceeds; the (“Payment Invoice”).

  • If the insurance certificate is for job-specific rather than annual coverage, a separate certificate MUST be submitted for each Product Testing Agreement.

  • IT Staff Product Testing Contact Table IT Staff Product Testing Contact Section Primary Contact Additional IT Staff Resources 1.

  • Indus shall perform Product Testing and code, mark, inspect, and sample the Products in accordance with applicable law and reasonable commercial practices.

Related to Product Testing

  • Manufacturing Site means a location where a manufacturing

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

  • Product Manufacturer means the entity that assembles the component parts to manufacture the final Product;

  • Drug use test means a scientifically substantiated method to test for the presence of illegal or performance-enhancing drugs or the metabolites thereof in a person’s urine.

  • Genetic testing means an analysis of genetic markers to exclude or identify a man as the father or a woman as the mother of a child. The term includes an analysis of one or a combination of the following:

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

  • Drug test means a test designed to detect the illegal use of a controlled substance.

  • 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.

  • Cannabis product means cannabis that has undergone a process whereby the plant material has been transformed into a concentrate, including, but not limited to, concentrated cannabis, or an edible or topical product containing cannabis or concentrated cannabis and other ingredients.

  • Collaboration Product means a pharmaceutical product containing or comprising Compound in any dosage form alone, or in combination with, one or more other pharmaceutically active ingredients, and any and all Improvements thereto.

  • Hemp product means the same as that term is defined in § 3.2-4112.

  • Collaboration Compound means any of the following: (a) FG-4592, (b) any HIF Compound (other than FG-4592) that is added to this Agreement pursuant to Section 3.6, and (c) any salts, esters, complexes, chelates, crystalline and amorphous morphic forms, pegylated forms, enantiomers (excluding regioisomers), prodrugs, solvates, metabolites and catabolites of any of the foregoing ((a) or (b)).

  • API means American Petroleum Institute.

  • Screening Test means a drug or alcohol test which uses a method of analysis allowed by the Minnesota Drug and Alcohol Testing in the Workplace Act to be used for such purposes.

  • 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.

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • Phase I Clinical Study means, as to a particular Licensed Product, an initial clinical study in humans with the purpose of assessing the Licensed Product’s safety, tolerability, toxicity, pharmacokinetics or other pharmacological properties.

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

  • Product Labeling means, with respect to a Licensed Product in a country or other jurisdiction in the Territory, (a) the Regulatory Authority-approved full prescribing information for such Licensed Product for such country or other jurisdiction, including any required patient information, and (b) all labels and other written, printed, or graphic matter upon a container, wrapper, or any package insert utilized with or for such Licensed Product in such country or other jurisdiction.

  • product type means any of the following:

  • Manufacturing operation means a process in which materials are changed, converted, or transformed into a different state or form from which they previously existed and includes refining materials, assembling parts, and preparing raw materials and parts by mixing, measuring, blending, or otherwise committing such materials or parts to the manufacturing process. "Manufacturing operation" does not include packaging.

  • Phase I Study means a study in humans which provides for the first introduction into humans of a product, conducted in healthy volunteers or patients to obtain information on product safety, tolerability, pharmacological activity or pharmacokinetics, as more fully defined in 21 C.F.R. § 312.21(a) (or the non-United States equivalent thereof).

  • Final Product means a product that is not used in producing other products and is built and intended for use outdoors, provided the final product has not deteriorated or has otherwise become a potential source of contaminants.

  • Investigational Medicinal Product means the study drug or control material as defined in the Protocol.

  • Remanufacturing means the activity of overhauling, retrofitting, fabricating, or repairing a product or its component parts for ultimate sale at retail.

  • Investigational Product means the Study Drug identified above and the control material, as further detailed in the Protocol;