Program of Studies Sample Clauses

Program of Studies. The student has 4.5 years to complete the program of study. Students are to assume professional responsibility and accountability for meeting program and course requirements including attendance and make-up. Each course identifies specific requirements to be met in order to achieve satisfactory completion of the course. All requirements need to be met in order to graduate. Students desiring to take a course at another institution during break or off-school hours must have permission from Recruitment, Admissions and Progression Committee before transfer credits will be received. Repeated tardiness, excessive absenteeism, rude behaviors and unprofessional behaviors are not acceptable. Tardiness or absence for any reason requires appropriate notification to the School of Nursing prior to the planned class or clinical experience. Absence without appropriate notification in which an examination or quiz has been scheduled will mean an automatic grade of “zero” for that examination or quiz. Clinical and nursing lab absences may require a make-up experience and a fee will be assessed. The fee must be paid prior to the make-up date. All absences that occur shall be discussed with the instructor involved in the planned experience. The student has the responsibility to see the instructor within 48 hours. The instructors(s) evaluate each student’s performance in relation to the course outcomes. If it is deemed necessary, the instructor(s) shall recommend faculty action to be taken regarding the absenteeism or tardiness. A student who is unable to meet the outcomes of the course due to absenteeism or repeated tardiness may be terminated.
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Program of Studies. Nr. i Indeksit Niveli i Studimeve (Bachelor apo Master) Viti Student ID No. Level of Studies (Undergrad or Grad) Year Me nënshkrimin e këtij dokumenti, unë dëshmoj se me xxxxxxx xxxxx xxx vendosur të jem pjesë e këtij programi/udhëtimi dhe xx xxx lexuar me kujdes dhe se i kam kuptuar në xxxxxx xx gjitha rregullat/kriteret/kushtet e pjesëmarrjes në këtë udhëtim sic xxxx definuar në dokumentin mbi Rregullat dhe Kriteret, Udhëtimi Studimor në SHBA. Unë, po ashtu, i pranoj të gjitha rregullat dhe kriteret e pjesëmarrjes në këtë udhëtim dhe shprehë gatishmërinë, përkushtimin, dhe pohimin xxx për t’iu përmbajtur të njejtëva pa asnjë rezervë. By signing this document, I do admit that I have willingly decided to participate in this program/study tour and that I have carefully read and fully understood all of the rules/criteria/terms and conditions of participation in this study tour as defined in the Terms and Conditions document of the USA Study Tour 2013. I do also accept and commit to respect all of the Terms and Conditions associated with this study tour. Nënshkrimi Data (dd/mm/vvvv) Signature Date (dd/mm/yyyy) Për shënime zyrtare: For office use only: Ulpiana, Rr. Xxxxxx Xxxxxx, 19/21 ♦ Prishtina 10000 ♦ Kosova
Sample 1
Program of Studies a. Students from XYZ will be placed in the regular undergraduate program at MU provided they meet all prerequisites for a particular course, as long as the course limits have not been reached and the individual Department/College allows enrollment of students from XYZ.
Sample 1

Related to Program of Studies

  • Clinical Trials The studies, tests and preclinical and clinical trials conducted by or on behalf of, or sponsored by, the Company, or in which the Company has participated, that are described in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus, or the results of which are referred to in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus, were and, if still pending, are being conducted in all material respects in accordance with protocols, procedures and controls pursuant to, where applicable, accepted professional and scientific standards for products or product candidates comparable to those being developed by the Company and all applicable statutes, rules and regulations of the FDA, the EMEA, Health Canada and other comparable drug and medical device (including diagnostic product) regulatory agencies outside of the United States to which they are subject; the descriptions of the results of such studies, tests and trials contained in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus do not contain any misstatement of a material fact or omit a material fact necessary to make such statements not misleading; the Company has no knowledge of any studies, tests or trials not described in the Disclosure Package and the Prospectus the results of which reasonably call into question in any material respect the results of the studies, tests and trials described in the Registration Statement, the Time of Sale Disclosure Package or Prospectus; and the Company has not received any notices or other correspondence from the FDA, EMEA, Health Canada or any other foreign, state or local governmental body exercising comparable authority or any Institutional Review Board or comparable authority requiring or threatening the termination, suspension or material modification of any studies, tests or preclinical or clinical trials conducted by or on behalf of, or sponsored by, the Company or in which the Company has participated, and, to the Company’s knowledge, there are no reasonable grounds for the same. Except as disclosed in the Registration Statement, the Time of Sale Disclosure Package and the Prospectus, there has not been any violation of law or regulation by the Company in its respective product development efforts, submissions or reports to any regulatory authority that could reasonably be expected to require investigation, corrective action or enforcement action.

  • Marketing Plan The MCP shall submit an annual marketing plan to ODM that includes all planned activities for promoting membership in or increasing awareness of the MCP. The marketing plan submission shall include an attestation by the MCP that the plan is accurate is not intended to mislead, confuse or defraud the eligible individuals or ODM.

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