Study tour definition

Study tour means a trip or tour taken by a group of people in order to study something, such as a language.
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Study tour means tour arranged during the course by the Principal outside the headquarters and excludes the journey time.
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Study tour means a symposium, seminar or study tour, except a study and training, organized for a period not exceeding Six months.
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Examples of Study tour in a sentence

  • Study tour to an industrial/business centre will form part of curriculum.

  • Study tour / field trips / excursions / picnics are arranged by the department, and students may participate in the same.

  • The possible training and capacity building actions include:• Study tour to Cape Town to learn experiences (has already been decided on);• Study tour to Vilnius.

  • Study tour to an Industrial or Business centre will form part of curriculum .The fourth / fifth semester BBA students of regular colleges shall be taken, under the supervision of faculty members, to a Business or Industrial centre so as to enable them to have firsthand knowledge about location, and operations of the Business or Industry .

  • CONTENT:1) Vacation Assignment/ Study tour is to be undertaken after the end of II semester exam and before the commencement of III semester classes.

  • Study tour( to Japan) in combination with desk study about the experience of relevant countries who are the member of GBIF.- Step 2: Understand the motivation of Viet Nam for joining GBIF:The first task for this group of stakeholders is to define the long term vision, goals and missions for the Participant Node; focus should be on how the Node willaddress the needs and priorities of Viet Nam, and how it will complement with other biodiversity‐related or information‐related initiatives.

  • Contents of the Study tour should therefore be tailored to the expectations of the study tour participants, concerning their demand for information and concrete topics to be discussed so that the participants reveice information that would benefit them the most in terms of practical utilization and future potential for achieving significanbt positive effects.

  • Activities include an agreement of cooperation with the Institute of Agricultural Research for the State of Parana to transfer no-till technology to farmers in the region of Campos Gerais, facilitation of the first World Bank Study tour and promote the no-tillage practice for soil conservation; and fostering the increase of small farm use of no-tillage technique.

  • Study tour Project Management (Component 4)1.Establishment of a Monitoring and Evaluation System 2.GIS mapping of intensive agricultural municipalities3.Technical assistance, training workshops, and equipment for performance-based I&D MIS4.Strengthening procurement and financial management capacity at all levels ANNEX 2.

  • Study tour participants also saw how, rather than relying on government bureaucracy to take the first step on priority issues, these CSOs were able to hold government more accountable for supporting change by pro-actively organizing meetings, proposing solutions and inviting government to participate.


More Definitions of Study tour

Study tour means the tour(s) arranged during the course by the Director outside the Headquarters.
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Study tour means a tour or visit to a country I city abroad, counties and I or states on the African Continent aimed at gathering knowledge and information regarding aspects of mutual interest concerning local government;
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Study tour means a workshop, seminar or observation tour to be organized for a period not exceeding Six weeks, other than a study and training.
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Related to Study tour

  • Study Site means the location(s) under the control of the Institution where the Study is actually conducted as set out in Schedule 1.

  • Study Completion means the database for the Study has been locked and all Essential Documents have been provided to the Sponsor, including a copy of the letter from the Reviewing HREC acknowledging receipt of the final report and/or closure letter from the Principal Investigator.

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

  • Bioassay means the determination of kinds, quantities or concentrations and, in some cases, the locations of radioactive material in the human body, whether by direct measurement, in vivo counting, or by analysis and evaluation of materials excreted or removed from the human body. For purposes of these rules, “radiobioassay” is an equivalent term.

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

  • 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;

  • Study Materials means all the materials and information created for the Study, or required to be submitted to the Sponsor including all data, results, Biological Samples, Case Report Forms (or their equivalent) in whatever form held, conclusions, discoveries, inventions, know-how and the like, whether patentable or not, relating to the Study, which are discovered or developed as a result of the Study, but excluding the Institution’s ordinary patient records.

  • Breath Alcohol Technician (BAT) means an individual who instructs and assists individuals in the alcohol testing process and who operates the EBT.

  • Phase III means human clinical trials, the principal purpose of which is to establish substantial evidence of both safety and efficacy in patients with the disease or condition being studied, as more fully defined in 21 C.F.R. §312.21(c) or similar clinical study in a country other than the United States. Phase III shall also include any other human clinical trial intended to serve as a pivotal trial to support the submission of an application for regulatory approval.

  • 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 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).

  • Study Data shall have the meaning set forth in Section 8.1.

  • Basic research means any original investigation for the advancement of scientific or technological knowledge that will enhance the research capacity of this state in a way that increases the ability to attract to or develop companies, jobs, researchers, or students in this state.

  • scientific research means any activity in the field of natural or applied science for the extension of knowledge;

  • Phase 1 Study means a clinical study of a drug candidate in human patients with the primary objective of characterizing its safety, tolerability, and pharmacokinetics and identifying a recommended dose and regimen for future studies as described in 21 C.F.R. §312.21(a), or a comparable clinical study prescribed by the relevant Regulatory Authority in a country other than the United States. The drug candidate can be administered to patients as a single agent or in combination with other investigational or marketed agents.

  • Development Work means any work carried out in relation to the physical construction of a mine;

  • 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.

  • Phase II Trial means a clinical trial of a Licensed Product on patients, including possibly pharmacokinetic and dose ranging studies, the principal purposes of which are to make a preliminary determination that such Licensed Product is safe for its intended use and to obtain sufficient information about such Licensed Product’s efficacy to permit the design of further clinical trials, and generally consistent with 21 CFR §312.21(b), or its successor regulation, or the equivalent in any foreign country.

  • Phase 3 Trial means a human clinical trial of a Product on a sufficient number of subjects 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 trial is intended to support Approval of a Product, as described in 21 C.F.R. 312.21(c) for the United States, or a similar clinical study prescribed by the Regulatory Authorities in a foreign country.

  • clinical investigation means any systematic investigation in one or more human subjects, undertaken to assess the safety or performance of a device;

  • Laboratory or “LANL” means the geographical location of Los Alamos National Laboratory, a federally funded research and development center owned by the DOE / NNSA.

  • Phase 2 Clinical Trial means a human clinical trial, for which the primary endpoints include a determination of dose ranges or an indication of efficacy in patients being studied as described in 21 C.F.R. §312.21(b), or an equivalent clinical trial in a country in the Territory other than the United States.

  • Phase I Clinical Trial means a human clinical trial that is intended to initially evaluate the safety and/or pharmacological effect of a Product in subjects or that would otherwise satisfy requirements of 21 C.F.R. 312.21(a), or its foreign equivalent.

  • Screening Test Technician (STT) means anyone who instructs and assists individuals in the alcohol testing process and operates an ASD.

  • 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).

  • 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.