Product Error definition

Product Error means undeclared behavior of the Product.
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Product Error means undeclared behavior of the Product or Services.
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Examples of Product Error in a sentence

  • Section 6.01 Copyrights and Ownership of Work Product Error! Bookmark not defined.Section 6.02 Patents and Inventions Error! Bookmark not defined.Section 6.03 Pre-existing Rights Error! Bookmark not defined.Section 6.04 Antitrust Error! Bookmark not defined.

  • PTV Support at a glance: 🠶 Any Product Error is to be reported to PTV’s global Helpdesk portal under xxxxx://xxxxxxxx.xxxxxxxx.xxx/ 🠶 Commercial questions or general queries xxxxx://xxx.xxxxxxxx.xxx/en/solutions Services provided by PTV beyond the scope of Product Support and Service Availability, for instance training, software development, consulting, etc, are not part of this SLA and shall be regulated by another specific agreement.

  • Accountability Procedures for the Study Product Error! Bookmark notdefined.

  • When providing Product Maintenance, Supplier shall respond to any unplanned interruption in the performance of the Products or any error, malfunction or degradation that results in the Products not conforming to the warranties in this Agreement (collectively, " Product Error"), by repairing or replacing the Products or components thereof, at its own cost and expense, in accordance with the process, timeframes and performance requirements set out in the Product Documentation.

  • Dosage, Preparation and Administration of Study Product Error! Bookmarknot defined.

  • PTV Support at a glance:  Any Product Error is to be reported to PTV’s global Helpdesk portal under xxxxx://xxxxxxxx.xxxxxxxx.xxx/  Commercial questions or general queries xxxxx://xxx.xxxxxxxx.xxx/en/solutions Services provided by PTV beyond the scope of Product Support and Service Availability, for instance training, software development, consulting, etc, are not part of this SLA and shall be regulated by another specific agreement.

  • CertiPath may correct such Product Error solely by amending the Product Documentation, or by fixing the Product Error in the current release of the Product.

  • Product analysis19Core Benefit Error! Bookmark not defined.Basic Product Error! Bookmark not defined.Expected Product Error! Bookmark not defined.Augmented Products Error! Bookmark not defined.Potential Products Error! Bookmark not defined.

  • Mr. Stanford for instance contested what he considers to be a commonly held belief that free trade is a sufficient condition to improve Canada’s trade performance; in his view, this belief undermines governments’ role in helping to build and strengthen priority sectors.

  • Raw materials required along with estimated quantity, likely source, marketing area of final products/s, Mode of transport of raw Material and Finished Product Error! Bookmark not defined.

Related to Product Error

  • Medication error means any preventable event that may cause or lead to inappropriate medication use or patient harm, while the medication is in the control of the health care professional, patient, or consumer. Such events may be related to professional practice, health care products, procedures, and systems including, but not limited to: prescribing; order communication; product labeling, packaging and nomenclature; compounding; dispensing; distribution; administration; education; monitoring; and use.

  • 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.

  • NAV Error means an error in the computation of the net asset value for a Fund or class as more fully described in the NAV Error Policy.

  • Product Data are illustrations, standard schedules, performance charts, instructions, brochures, diagrams, and other information furnished by the Contractor to illustrate materials or equipment for some portion 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.

  • Product Know-How means Know-How

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

  • API means American Petroleum Institute.

  • Defective Product has the meaning set forth in Section 5.2.

  • Manifest Error means any error that we reasonably believe to be obvious or palpable, including without limitation, offers to execute Transactions for exaggerated volumes of Underlying Assets or at manifestly incorrect market price quotes or prices at a clear loss.

  • Manufacturer means a person who:

  • Product Group or “the Group” means a group of lotteries that has joined together to offer a product pursuant to the terms of the Multi-State Lottery Agreement and the Product Group’s own rules.

  • Active Pharmaceutical Ingredient or “API” means the active pharmaceutical or biological ingredient as further set forth in the applicable Product Manufacturing Plan.

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

  • 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;

  • Product Specification means a file attached to the application for the protection of a geographical indication, in which the specifications with which the spirit drink has to comply are set out, and which was referred to as a ‘technical file’ under Regulation (EC) No 110/2008;

  • Program Materials means the documents and information provided by the Program Administrator specifying the qualifying EEMs, technology requirements, costs and other Program requirements, which include, without limitation, program guidelines and requirements, application forms and approval letters.

  • Active Ingredient means any com- ponent that is intended to furnish pharmacological activity or other di- rect effect in the diagnosis, cure, miti- gation, treatment, or prevention of dis- ease, or to affect the structure or any function of the body of humans. The term includes those components that may undergo chemical change in the manufacture of the drug product and be present in the drug product in a modified form intended to furnish the specified activity or effect.