Technical study definition

Technical study means a geologic or hydrologic report prepared and published by a state or federal agency, or a study published in a peer-reviewed scientific journal, or a report prepared and signed by a professional geologist or by a professional engineer.
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Technical study means technical studies including, inter alia: (i) an environmental assessment including an evaluation of alternative options; (ii) architectural studies including un schéma directeur de l’espace; and (iii) engineering studies including physical access to the campus and to individual buildings, water, electricity supply and waste removal;
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Technical study. Establishment of a Caribbean Centre of Excellence for Financial Services in The Bahamas Barbados • Enhancing the Export Capacity of Cultural Entrepreneurs in Barbados • Enhancement of Food Safety and Quality Infrastructure in the Condiments Sub-Sector of Barbados Belize • Enhancing the National Quality Infrastructure of Belize • Enhancing the Resilience of the Citrus Sector: Accreditation of The Citrus Research and Educational Institute (CREI) Laboratory and ISO 9001:2008 Certification for the Plant World Nursery Dominica • Enhancing Dominica’s Trading Environment and Export Capacity • Building Capacity for Effective Consumer Protection in Dominica Dominican Republic • Improving the Dominican Republic’s EPA Implementation Capacity Grenada • Enhancing the Capacity of Grenada to Export Fresh Fruit to the EU and CARIFORUM Markets • Enhancing the Capacity of Grenadian Nationals to Take Advantage of CSME Guyana • Improving Competitiveness in Guyana And Strengthening of SMES to Increase Non-Traditional Exports • Institutional Strengthening of the National Accreditation Council (NAC) Of Guyana • Institutional Strengthening of the Council for Technical and Vocational Education and Training (CTVET), Guyana Jamaica • Establishment of the Bureau of Standards Packaging Laboratory St. Kitts and Nevis • Enhancing the National Quality Infrastructure of St. Kitts And Nevis • Enhancing the National Statistical System of St. Kitts And Nevis Saint Lucia • Developing Saint Lucia’s Services Sector • Enhancing Saint Lucia’s Trading Environment and Export Capabilities St. Xxxxxxx and the Grenadines • Building Export Capacity and Improving Competitiveness in the Services Sector • Enhancing the Capacity of St. Xxxxxxx and the Grenadines’ Nationals to Take Advantage of CSME Suriname • Feasibility Study for the Technical, Financial and Legal Requirements for the Establishment of an Electronic Single Window Facility • Developing the Export-Readiness of Suriname’s Agrifood Enterprises for The CARICOM Market Trinidad and Tobago • Developing the Export Readiness of Trinidad and Tobago’s Enterprises for the EU Market • Development of a National Quality Policy for Trinidad and Tobago Editor: Xxxxxx Xxxxxx
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Examples of Technical study in a sentence

  • Technical study tours will undertaken as part of the training activities, closely linked to the next Output on knowledge management and exchange, to locations selected for their applicability to the Samoan context.

  • DJB, through JICA Technical study, has framed Master Plan for water supply 2021 based on water demand of all areas.

  • Batteries mapped to LCR areas will be prioritized based on the CAISO’s 2030 Local Capacity Technical study results33, which show the level of 4-hour battery storage that can provide both system and local capacity value within each LCR area.

  • Technical study of this project is being conducted and is due to be completed by end of 2016.

  • Technical study tour to Mozambique (visit at FIPAG, CRA and AIAS).

  • Technical study, for all subprojects, will be conducted by the EA including its cost estimate.

  • JICA Technical study aims to develop action plan for commissioning SCADA in the entire network and execute the pilot SCADA in Bhagirathi WTP and its command area.

  • Technical study may be required to determine the shoreline hazard limit as part of any planning and development application.

  • DJB, through JICA Technical study, is framing Master Plan for water supply based on various raw water scenarios, GIS mapping and water demand of all areas.

  • Final Report 1997 [4] PreussenElektra: Technical study of the conditions for joint operation of the extended UCPTE system and power systems of the Oriental Europe and Central Asia.


More Definitions of Technical study

Technical study means a detailed technical report in form and substance sufficient to permit the Owners, acting reasonably, to make a decision to bring a deposit of Minerals in the Bellekeno Mining Properties into commercial production, and showing that the placing of any part of the Bellekeno Mining Properties into commercial production is feasible and should be profitable and will include a reasonable assessment of all relevant issues including, the various categories of ore reserves and resources and their amenability to metallurgical treatment, a complete description of the work, equipment and supplies required to bring such part of the Bellekeno Mining Properties into commercial production and the estimated cost thereof, a description of the mining methods to be employed and a financial appraisal of the proposed operations and including, without limitation, the following:
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Related to Technical study

  • Clinical Study means a Phase I Study, Phase II Study, Phase III Study, or Pivotal Study, as applicable; but excluding any Post-Approval Studies.

  • Clinical Studies means human clinical trials for a Licensed Product and any other tests and studies for a Licensed Product in human subjects.

  • Phase I Clinical Study means a human clinical study of a product, the principal purpose of which is a preliminary determination of safety in healthy individuals or patients, as described in 21 C.F.R. 312.21(a).

  • 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 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).

  • Phase III Clinical Study means a human clinical study of a product on a sufficient number of subjects that is designed to establish that such product is safe and efficacious for its intended use, and to determine warnings, precautions, and adverse reactions that are associated with such product in the dosage range to be prescribed, which trial is intended to support Regulatory Approval of such product, as described in 21 C.F.R. 312.21(c). 1.185. [***] 1.186. [***]

  • 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.

  • Study means the investigation to be conducted in accordance with the Protocol.

  • 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.

  • Pivotal Study means (a) a Phase 3 Study that is intended by Celgene to be submitted (together with any other registration trials that are prospectively planned when such Phase 3 Study is initiated) for Regulatory Approval in the U.S. or the EU, or (b) any other clinical study that is designed to establish that a pharmaceutical product is safe and efficacious for its intended use, and to determine warnings, precautions, and adverse reactions that are associated with such pharmaceutical product in the dosage range to be prescribed, which clinical study is a registration trial intended to be sufficient for filing an application for a Regulatory Approval for the Licensed Product in the U.S. or another country or some or all of an extra-national territory, solely as evidenced by the acceptance for filing for a Regulatory Approval for such product after completion of such study.

  • 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;

  • Development Plan has the meaning set forth in Section 3.2.

  • 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 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 I Clinical Trial means a clinical trial conducted in healthy humans or patients, which clinical trial is designed to establish the safety, drug-drug interactions and/or pharmacokinetics of an investigational drug given its intended use, and to support continued testing of such drug in Phase II Clinical Trials.

  • Development Work means the work of development to be performed on or with respect to the Land (including, without limitation, the installation of utilities, roads and all related on-site and off-site improvements) in connection with the development of the Land for the subsequent construction thereon of Homes, all of which work and construction shall be completed by or on behalf of the Borrower in accordance with the Plans and Specifications, but shall not include the Construction Improvements.

  • 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.

  • 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).

  • Phase 4 Clinical Trial means a Clinical Trial of a Product conducted after Regulatory Approval of such Product has been obtained from an appropriate Regulatory Authority, which trial is (a) conducted voluntarily by a Party to enhance marketing or scientific knowledge of the Product, or (b) conducted due to a request or requirement of a Regulatory Authority.

  • Pivotal Clinical Trial means, with respect to a Licensed Product, (a) a phase 3 Clinical Trial or (b) any other clinical trial that is intended (as of the time the study is initiated) to obtain the results and data to support (without the need to conduct any additional clinical trial) the filing of an application for Regulatory Approval for such product.

  • Development Phase means the period before a vehicle type is type approved.

  • Development Candidate means a Collaboration Compound designated by Biogen Idec as a Development Candidate in accordance with Section 2.6.

  • Phase II Clinical Trial means a controlled human clinical study that would satisfy the requirements of 21 CFR 312.21(b), conducted to study the effectiveness and establish the dose range of a Product for a particular Indication in patients with the disease or condition under study, including a Phase IIA Clinical Study or Phase IIB Clinical Study.

  • Phase III Clinical Trial means a human clinical trial, the principal purpose of which is to demonstrate clinically and statistically the efficacy and safety of a Licensed Product for one or more indications in order to obtain Marketing Approval of such Licensed Product for such indication(s), as further defined in 21 C.F.R. §312.21 or a similar clinical study in a country other than the United States.

  • System Impact Study means an assessment by the Transmission Provider of (i) the adequacy of the Transmission System to accommodate a Completed Application, an Interconnection Request or an Upgrade Request, (ii) whether any additional costs may be incurred in order to provide such transmission service or to accommodate an Interconnection Request, and (iii) with respect to an Interconnection Request, an estimated date that an Interconnection Customer’s Customer Facility can be interconnected with the Transmission System and an estimate of the Interconnection Customer’s cost responsibility for the interconnection; and (iv) with respect to an Upgrade Request, the estimated cost of the requested system upgrades or expansion, or of the cost of the system upgrades or expansion, necessary to provide the requested incremental rights. System Protection Facilities: “System Protection Facilities” shall refer to the equipment required to protect (i) the Transmission System, other delivery systems and/or other generating systems connected to the Transmission System from faults or other electrical disturbance occurring at or on the Customer Facility, and (ii) the Customer Facility from faults or other electrical system disturbance occurring on the Transmission System or on other delivery systems and/or other generating systems to which the Transmission System is directly or indirectly connected. System Protection Facilities shall include such protective and regulating devices as are identified in the Applicable Technical Requirements and Standards or that are required by Applicable Laws and Regulations or other Applicable Standards, or as are otherwise necessary to protect personnel and equipment and to minimize deleterious effects to the Transmission System arising from the Customer Facility. Transmission Facilities:

  • Phase I Trial means a clinical trial of a Licensed Product in human patients conducted primarily for the purpose of determining the safety, tolerability and preliminary activity of the Licensed Product, including, without limitation, for determining the maximum tolerated dose, or optimal dose. For purposes of this Agreement, a Phase I trial shall specifically exclude a study in healthy volunteers.