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The TU "IRB Approval Process" Flowchart What Is Human Subjects Research? Is My Research "Reviewable Research"? U.S. FDA's IRB Information Website List of Web-Based Tutorials on Human Subjects Protection
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What is the IRB? The use of human subjects in Towson University faculty, staff or student research requires approval by the appropriate University review committee. This committee, the IRB, appointed by the President, is comprised of volunteers from Towson University's faculty and staff and at least one member of the community. The current chair of Towson University's IRB is Dr. Debi Gartland, Professor of Special Education. The IRB is responsible for reviewing research involving human subjects to ensure compliance with all governmental regulations with the use of human subjects. Approval of the IRB must be obtained PRIOR to the involvement of human subjects in research, and for any modifications to the project after IRB approval which would impact the human participants. Applicable federal regulations are detailed in Title 45 of the Code of Federal Regulations, Part 46. Questions? The Office of Sponsored Programs & Research is the first point of contact regarding human subjects research at or involving Towson University faculty, staff, or students. Phone: 410-704-2236, or email: ours@towson.edu.
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