Research Subjects
Review Board
"... to protect the rights and welfare of human research subjects at the
University of Rochester. To accomplish this, we review, approve the initiation of,
and conduct periodic review of research involving human subjects."
Research Education
and Training
Next Seminar... October 15,2013
Next Workshop... 3 Day Workshop
ROSS Training .... RSRB ROSS training 3rd Monday of every month from 2pm to 3pm. Please Click HERE to sign up.
Quality Improvement
"To assess and assist the Investigator (PI) in assuring the rights and wellbeing of human subjects are protected and that the study is being conducted in accordance with IRB requirements, the approved protocol, applicable Federal regulations, U of R policies and best practice (GCP) standards."Research Subjects Review Board
The University of Rochester, by action of the President and Board of Trustees, has established a system of institutional review boards to review research. These boards, each with the title of Research Subjects Review Board (RSRB), are supported by a staff office (RSRBO). The RSRBs review research that is conducted or supported by the University of Rochester to determine that the rights and welfare of the human subjects are adequately protected. The RSRB is guided by the ethical principles described in the Belmont Report and by the regulations of the U.S. Food and Drug Administration (21 CFR 50 and 56) and the U.S. Department of Health and Human Services (45 CFR 46). The University of Rochester maintains an Assurance of Compliance with the Office for Human Research Protection (OHRP).
Contact the RSRB Office at (585) 275-3050 with any questions.
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Policies/Guidance
Document Templates
Applying to WIRB
- WIRB or RSRB Review
- WIRB Submission Process
- Change in Study Responsibility
- WIRB.com
- WIRB Fee Schedule
- WIRB IRB of Record
