Study Program definition

Study Program means the program to be produced and carried out by the Contractor in accordance with Article 9 following the conclusion that Commercial Production is feasible.
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Study Program means the study program detailed in the Application Form and undertaken by the Recipient under this Agreement to achieve the Grant Objectives in compliance with the Healthway Objective;
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Study Program means the overseas study devised for the applicant and for which the applicant seeks a grant from the AETT.
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Examples of Study Program in a sentence

  • The recommended study plan was prepared and approved within the Study Program Council, while the guarantors of individual courses, employers and students also commented on it.

  • There are two options to satisfy the requirements of the DMR-QA Study Program: (1) The Discharger can obtain and analyze a DMR-QA sample as part of the DMR-QA Study; or (2) Per the waiver issued by U.S. EPA to the State Water Board, the Discharger can submit the results of the most recent Water Pollution Performance Evaluation Study from its own laboratories or its contract laboratories.

  • A completed petition for the Reduced Fee Part-Time Study Program approved by the Departmental Faculty Graduate Advisor (and Associate Dean, if required by the school), and a memo from the Graduate Advisor in support of the request must be submitted to the Graduate Dean.

  • The results will be continuously evaluated by the Study Program Board at the Faculty of Medicine, and the results will be submitted to the Accreditation Council of the Faculty of Medicine, the Board for Quality of the Faculty of Medicine and the management of the Faculty of Medicine.

  • The internal system is issued in accordance with the Standards for the Internal Quality Assurance System of Higher Education (hereinafter referred to as the “Internal System Standards”) and the Study Program Standards (hereinafter referred to as the “Study Program Standards”) issued by Slovak Accreditation Agency for Higher Education (hereinafter referred to as "SAAVŠ").

  • Any study fees paid to the University for the Study Program in excess of the aforementioned amount shall be reimbursed.

  • Proceedings also can be accessed online on the website http://eprints.perbanas.ac.id/ Chair of the Master Management Study Program Universitas Hayam Wuruk Perbanas Prof.

  • Prior rule § 6(I) provided the Board had discretion to “allow an applicant partial credit for study which does not meet with the minimum requirements prescribed by this section as the Board shall deem just and equitable.” Because § 6 addressed several types of prescribed study, and § 6(j) provided certain limited options for credit for the Law Office Study Program, the scope of § 6(l) was not entirely clear.

  • The 4th International Conference on Business and Banking Innovations was held on 29th January 2022 by virtual (online) zoom meeting and organized by the Master Management Study Program of Universitas Hayam Wuruk Perbanas in Collaboration with five Higher Education Institutions in Indonesia and three Universities from Asia countries.

  • The provisions of new Rule 7(e) (drawn from § 6(j)) set forth the recognized bases for granting credit toward the four- year term for the Law Office Study Program.


More Definitions of Study Program

Study Program. English Education Study Program Title : Students’ attitude towards English Speaking at eight grade students of MTS An-nur Tangkit Islamic boarding school Muaro Jambi
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Study Program. English Education Study Program Title : Students’ attitude towards English Speaking at Eight Grade Students of MTS An-nur Tangkit Islamic Boarding School Muaro Jambi TABLE OF CONTENTS COVER OFFICIAL NOTE i THESIS APPROVAL iii ORIGINAL THESIS STATEMENT iv DEDICATION v MOTTO vi ACKNOWLEDGEMENT vii ABSTRACT ix TABLE OF CONTENTS x LIST OF TABLE xiii LIST OF PICTURE xiv CHAPTER I INTRODUCTION 1
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Study Program means the program tailored to meet the needs of the Participant and as agreed with the Participant in discussion.
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Study Program means the proposed study program for the Casino Project, substantially in the form attached as Schedule “C”.
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Related to Study Program

  • Development Program means the implementation of the development plan.

  • Pilot program means the pilot program identified and funded through the Funding Agreement and described in that Funding Agreement and its attachments.

  • E-Verify Program above means the employment verification program administered by the United States Department of Homeland Security, the Social Security Administration, or any successor program.

  • Research Program has the meaning set forth in Section 3.1.

  • Program of study means a curriculum that requires a candidate to demonstrate and document competency in the specific knowledge, skills, and dispositions for a particular endorsement to an educator’s license, a licensure content area, or level of licensure, and is:

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

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

  • Program Plan means the tobacco settlement program plan dated February 14, 2001, including exhibits to the program plan, submitted by the authority to the legislative council and the executive council, to provide the state with a secure and stable source of funding for the purposes designated by section 12E.3A and other provisions of this chapter.

  • Development Plans means a coherent set of operations defined and financed exclusively by the OCTs in the framework of their own policies and strategies of development, and those agreed upon between an OCT and the Member State to which it is linked;

  • Marketing program means a program established by order of the director pursuant to this act prescribing rules and regulations governing the marketing for processing, distributing, selling, or handling an agricultural commodity produced in this state or agricultural commodity input during a specified period and

  • 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.

  • 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 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 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 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).

  • Licensed Program means the executable processing programs of licensed information, which is composed of various modules in the Licensed Software package provided by the Licensor.

  • Training program means an NCA-approved Iowa college, the Iowa law enforcement academy or an Iowa hospital approved by the department to conduct emergency medical care training.

  • 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.

  • 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.

  • Development Activities means those activities which are normally undertaken for the development, construction, repair, renovation, rehabilitation or conversion of buildings for residential purposes, including the acquisition of property;

  • 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.

  • 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.

  • Phase IV Clinical Trial means a product support clinical trial of a Product commenced after receipt of Regulatory Approval in the country where such trial is conducted. A Phase IV Clinical Trial may include epidemiological studies, modeling and pharmacoeconomic studies, and investigator-sponsored clinical trials studying Product that are approved by the JDC and that otherwise fit the foregoing definition.

  • Commercialization Plan has the meaning set forth in Section 6.2.

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

  • AML Program has the meaning ascribed thereto in Schedule 2.1(F)(8) hereof.