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Welcome to the home page for the University of Houston's Committees for the Protection of Human Subjects (CPHS). The University of Houston is committed to the pursuit of excellence in teaching, research and public service. Concomitantly, the University seeks to protect the welfare of every person who may be involved in research and training projects in accordance with the federal regulations, 45 CFR 46 and the ethical principles established by the Belmont Report.
All UH faculty, staff or students who propose to engage in any research activity involving the use of human subjects must have approval prior to the initiation of the project from the CPHS. The CPHS is responsible for safeguarding of the rights and welfare of all persons participating in research projects, whether funded or non-funded.
Any questions regarding these Committees, policies and procedures related to human subjects research, etc. should be directed to the Office of Research Policies, Compliance, and Committees at (713) 743-9204.
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PROGRAMS, APPLICATIONS, FORMS OFFERED
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Application for New Protocol
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Appendix A - Request for Waiver of Documentation of Consent
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Appendix B - Request for Waiver of Informed Consent
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Meeting and Deadline Dates
If you are a faculty member or student in any department within the College of Liberal Arts and Social Sciences, CLICK HERE for the schedule for Committee 2.
If you are a faculty member or student in ALL other program areas (such as college of Education, Graduate School of Social Work), CLICK HERE for the schedule for Committee 1.
All CPHS materials submitted from the College of Optometry must have the approval of the college committee prior to submission to the Committee for the Protection of Human Subjects. This includes applications for new protocols or requests for revision. Renewal applications do not require the approval of the College Committee. Investigators are advised to check with the college committee to determine the appropriate deadlines.
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| Human Subjects Policies and Procedures for Research |
| Application for Renewal/Final Report |
| Frequently Asked Questions |
| Application for Revision to a Currently Approved Protocol |
| Reportable Event Form for Adverse/Unanticipated Events |
| Exempt Categories |
| Expedited Categories |
| Information about Informed Consent |
| CITI Human Subjects Research Educational Program |
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