Field trials definition

Field trials means the using or working of dogs or raptors that are being tested or judged in their performance in finding, tracking, trailing, pointing, hunting or retrieving game birds, by persons other than the owner or handler.
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Field trials means a field experiment of growing a genetically engineered organism in the environment under specified terms and conditions which are intended to mitigate the establishment and spread of the organism;
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Field trials means the test procedures used and services provided to evaluate the performance of the Prototypes as integrated into the Crown Infrastructure.
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Examples of Field trials in a sentence

  • The parties shall conduct field trials for the Products ("Field Trials") pursuant to the Field Trial Agreement attached hereto as Exhibit B.

  • In the event of such termination by Cisco following the demonstration of proof of concept as set forth in Section 6.1(b), Cisco shall return the $2 million development payment paid to Cisco upon demonstration of proof of concept and any payments by Ambient for the Field Trials, but Cisco shall be entitled to retain the $2 million payment made upon execution of this Agreement.

  • Calypso is in the process of developing a new business (the "Business") consisting of the licensing of certain proprietary technology and the manufacture and sale of certain wireless communications devices, and desires to retain the services of Consultant to assist Calypso in the development of the Company's Field Trials Kit documents.

  • For Orders that involve Field Trials, CINGULAR's Acceptance Test Period shall commence upon (i) CINGULAR's receipt of SUPPLIER's Notice of Completion, or (ii) upon CINGULAR's receipt of Material where SUPPLIER provides no Services other than shipping.

  • In the event of such termination by Cisco following the demonstration of proof of concept as set forth in Section 6.1(b), Cisco shall return the [***] development payment paid to Cisco upon demonstration of proof of concept and any payments by Ambient for the Field Trials, but Cisco shall be entitled to retain the [***] payment made upon execution of this Agreement.

  • Motorola will provide one (1) person at the Site during the tests to be conducted in Section 21.7.1 Support of Iridium's Initial ICRS Field Trials (Mobility Application Part (MAP) layer above.

  • Additional Value Creation Through Technical Initiatives to Improve Returns RigtelligentTM - Operating System Deploying across full AC fleet iRackerTM - Automated Tubular Handling System Prototype Testing Commercial build-out 2H 2017 Rotary Steerable System Performing Field Trials Commercial build-out 2017 14 Please refer to the disclaimers on slides 2 and 3 of the presentation deck.

  • Q2/Q3, 2018 Complete Field Trials of Near Surface HyperCore™ ($100,000: 20 x $5,000 / day trials) Trend InformationHyperSciences spent much of 2015 through 2017 focused on developing all aspects of HyperDrill™, for both conventional energy drilling and for deep geothermal drilling.

  • For Section 21.7.1 Support of Iridium's Initial ICRS Field Trials (Mobility Application Part (MAP) layer above, Motorola's support for final acceptance will end after the provision of 8 man months of labor or the Commercial Activation Date, whichever comes first.

  • After Trait Validation, Field Trials continue with customer specific Lines.


More Definitions of Field trials

Field trials means an Exhibition conducted by an Affiliate Member approved by Council to conduct Field Trials. “General Specials” means that part of the judging procedure where the best of Group winners compete for best in show awards.
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Related to Field trials

  • Field trip means any experience a child has away from the premises of the center, while under the care of center staff, whether a child walks or is transported.

  • Clinical Trials means a controlled study in humans of the safety or efficacy of a Product, and includes, without limitation, such clinical trials as are designed to support expanded labeling or to satisfy the requirements of an Agency in connection with any Product Approval and any other human study used in research and Development of a Product.

  • Clinical Studies means Xxxxx 0, Xxxxx 0, Xxxxx 0, Xxxxx 3, and such other tests and studies in human subjects that are required by Applicable Law, or otherwise recommended by the Regulatory Authorities, to obtain or maintain Regulatory Approvals for a Licensed Product for one (1) or more indications, including tests or studies that are intended to expand the Product Labeling for such Licensed Product with respect to such indication.

  • Clinical Study means a Phase I Study, Phase II Study, Phase III Study, as applicable.

  • 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.

  • Phase III Clinical Trials means a Clinical Trial for the Product on sufficient numbers of patients to generate safety and efficacy data to support Regulatory Approval in the proposed therapeutic indication, conducted in accordance with current good clinical practices and in accordance with a protocol that has been reviewed by the FDA and reflects any comments or concerns raised by the same.

  • Clinical means having a significant relationship, whether real or potential, direct or indirect, to the actual rendering or outcome of dental care, the practice of dentistry, or the quality of dental care being rendered to a patient;

  • 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)).

  • Clinical Trial means a Phase I Clinical Trial, Phase II Clinical Trial or Phase III Clinical Trial, or any post-approval human clinical trial, as applicable.

  • Phase 4 Clinical Trial means a Clinical Study in any country which is conducted after Regulatory Approval of a product has been obtained from an appropriate Regulatory Authority, consisting of trials conducted voluntarily for enhancing marketing or scientific knowledge of an approved indication and trials conducted due to request or requirement of a Regulatory Authority.

  • Phase I Clinical Trial means a study in humans which provides for the first introduction into humans of a product, conducted in normal volunteers or patients to generate information on product safety, tolerability, pharmacological activity or pharmacokinetics, or otherwise consistent with the requirements of U.S. 21 C.F.R. §312.21(a) or its foreign equivalents.

  • 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.

  • Research Use shall have the meaning given in Section 2.2.2 of this Agreement.

  • Collaboration Know-How means all Know-How conceived, discovered, developed or otherwise made by or on behalf of a particular Party or any of its Affiliates or permitted subcontractors of any of the foregoing (solely or jointly by or on behalf of a particular Party or any of its Affiliates or permitted subcontractors of any of the foregoing) in the course of [***].

  • Clinical Data means the information concerning the safety or performance that is generated from the use of a device and that are sourced from the following:

  • Phase 2 Clinical Trial means a human clinical trial of a product in any country that would satisfy the requirements of 21 C.F.R. 312.21(b) and is intended to explore a variety of doses, dose response, and duration of effect, and to generate initial evidence of clinical safety and activity in a target patient population, or a similar clinical study prescribed by the relevant Regulatory Authorities in a country other than the United States.

  • Commercialization or “Commercialize” means activities directed to marketing, promoting, research and development as required, manufacturing for sale, offering for sale, distributing, importing or selling a product, including sub-licensing or sub-contracting of these activities.

  • Field means [***].

  • Phase 1 Clinical Trial means a Clinical Trial of a Product on sufficient numbers of normal volunteers and/or patients that is designed to establish that such Product is safe for its intended use and to support its continued testing in Phase 2 Clinical Trials. For purposes of this Agreement, ‘initiation’ of a Phase 1 Clinical Trial for a Product means the first dosing of such Product in a human subject in a Phase 1 Clinical Trial.

  • Phase IIb Clinical Trial means a clinical trial of a Product on sufficient numbers of patients that is designed to provide a preliminary determination of safety and efficacy of such Product in the target patient population over a range of doses and dose regimens.

  • Collaboration has the meaning set forth in Section 2.1.

  • Phase 3 Clinical Trial means a pivotal clinical trial in humans performed to gain evidence with statistical significance of the efficacy of a product in a target population, and to obtain expanded evidence of safety for such product that is needed to evaluate the overall benefit-risk relationship of such product, to form the basis for approval of an NDA and to provide an adequate basis for physician labeling, as described in 21 C.F.R. § 312.21(c) or the corresponding regulation in jurisdictions other than the United States.

  • Phase II Clinical Study means a human clinical study of a product initiated to determine the safety and efficacy in the target patient population, as described 21 C.F.R. 312.21(b).

  • Licensed Territory means worldwide.

  • Phase III Clinical Study means a trial involving administration of a Compound to sufficient numbers of human patients with the goal of establishing that the Compound is safe and efficacious for its intended use, to define warnings, precautions and adverse reactions that are associated with the drug or label expansion of such Compound, and to be considered as a pivotal study for submission of an NDA.

  • Research Plan shall have the meaning set forth in Section 2.1.