Approved Program of Study definition

Approved Program of Study means a program of study approved for the purposes of Ontario Student Grants and Ontario Student Loans under the MTCUA.
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Approved Program of Study means a program of study approved in accordance with subsection 7 (1);
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Approved Program of Study means a program of study approved for student loan and other OSAP purposes pursuant to the Performance Requirements.
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More Definitions of Approved Program of Study

Approved Program of Study means a program of study approved for the purposes of Ontario Learn and Stay Grants under the MTCUA.
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Approved Program of Study means those child welfare- related undergraduate and graduate degree programs designated by the corporation on an annual basis and published on the corporation’s website conducted by an institution situated in the State, which has been approved and operating in this State for at least one year, and has been approved for participation in federal student financial aid programs authorized by Title IV of the Higher Education Act of 1965, as amended.
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Approved Program of Study means a program of study offered by an approved institution that satisfies the requirements of division (B) of this section.
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Approved Program of Study means a program of study approved in accordance with section 7; (“programme d’études approuvé”)
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Approved Program of Study means a program of study approved for student loan and other OSAP
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Approved Program of Study means a program of study approved in accordance with the regulations;
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Related to Approved Program of Study

  • 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:

  • Approved program or "approved state" means a state or interstate program that has been approved or authorized by EPA under 40 CFR Part 123 (2000).

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

  • 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).

  • 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.