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FACULTY HANDBOOK July 2009 - Morgan State University

FACULTY HANDBOOK July 2009 - Morgan State University

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PAGE 44 * <strong>Morgan</strong> <strong>State</strong> <strong>University</strong> Faculty Handbook2.12 Grade Change PolicyIt is <strong>University</strong> policy that once a grade is recorded, no changes are allowed.The only exceptions to this policy are as follows:(1) Incompletes - All incompletes must be removed by the end of the nextsemester of enrollment following the granting of an incomplete (“I”) grade.(2) Recording error(s) and/or miscalculationsof a grade must be changed no later than the end of the semester followingthe recording error or miscalculation. Grade changes must be approved bythe area Chairperson and Dean.NOTE:All changes under part (2) of this policy must be supported bydocumentation; i.e., grade books, papers and examinations and calculationrecords.2.13 The Institutional Review Board (IRB)/ Protection of Human ResearchParticipants<strong>Morgan</strong> <strong>State</strong> <strong>University</strong> policy on the protection of human researchparticipants requires that all research conducted under its auspices, whichinvolve human subjects, must be reviewed and approved by the InstitutionalReview Board (IRB), consistent with Federal Regulations, 45 CFR 46. TheIRB reviews research protocols (biomedical, social or behavioral)prospectively from the viewpoint of protecting the rights and safeguardingthe welfare of human research participants using the following criteria: (a)the design of the study is consistent with sound scientific principles andethical norms; (b) the protocol meets the National Institutes of Health (NIH)federal wide assurance ( FWA) criteria necessary for approval; (c) thenecessary elements of informed consent have been fulfilled; and (d)additional appropriate safe guards have been provided if potentiallyvulnerable subjects (e.g., pregnant women, neonates, children, prisoners, andfetuses) are to be studied.The IRB conducts continuing review of each approved protocol at leastannually. The IRB may modify, suspend or terminate approval of researchthat has been associated with serious harm to subjects, or is not beingconducted in accordance with the IRB’s decisions, stipulations orrequirements.Applications for IRB approval should include the following:(a) Completed and signed “Human Subjects Application Form”;(b) Project summary;(c) Research protocol;(d) Informed consent form; assent form (for minors); debriefing form;(e) Questionnaires, interview questions, tests, etc.

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