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
GCP Training - offered on-line through CITI...
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."HIPAA Authorization to Obtain Health Information
To ensure that the nine required elements of a HIPAA compliant authorization are contained in release of information requests, the Authorization Form SH 48 may not be altered, with the exception of the contact information in the upper right-hand corner. Please call Brenda Tryon at R.R. Donnelly at 249-7703 to provide the appropriate contact information for your study and to order the forms.
A sample of this form can be viewed here.
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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
