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Federal Wide Assurance
Wayne State University operates its Human Research Protection Program under a Federal Wide Assurance (FWA) on file with the Office for Human Research Protection with identification number: FWA 00002460. This registration can be accessed by typing in "Wayne State U" at this website: http://ohrp.cit.nih.gov/search/fwasearch.aspx?styp=bsc.
Individually Registered IRB Committee Numbers:
IRB00006856 is for PH1- Medical
IRB00000325 is for M1- Medical adult
IRB00000326 is for MP2- Medical and Pediatric
IRB00000327 is for B3- Social, Behavioral, Education, and
IRB00000328 is for MP4- Medical and Pediatric
This FWA covers the WSU IRBs and its affiliated health care institutions (Barbara Ann Karmanos Cancer Institute, Children's Hospital of Michigan, Detroit Receiving Hospital/University Health Center, Sinai-Grace Hospital, Harper University Hospital, Huron Valley/Sinai Hospital, Hutzel Women's Hospital, Rehabilitation Institute of Michigan, John D. Dingell Veterans Administration Medical Center, Michigan Orthopedic Surgery Hospital, and Oakwood Healthcare System).
For questions, concerns or suggestions regarding the Human Research Protection Program, please call (313) 577-1628.
- IRB Training - Retrospective Chart Reviews
- December 11 2013 at 1:00 PMScott HallA retrospective chart review (medical records) may serve as the primary method for data collection in a research project or a retrospective chart review may done to identify eligible participants for additional data collection. This session will offer details on the information the IRB is required to review for research involving retrospective chart reviews. The training will involve a discussion of both the Protocol Summary Form and HIPAA regulations that applies when accessing medical records. When: Wednesday, December 11, 2013, 1:00 pm– 2:00 pm Where: WSU School of Medicine, Scott Hall, Room 1140 Speaker: Ray-Nitra Pugh, Education Coordinator, IRB Administration Office
- IRB Training: Informed Consent Process – WEBINAR
- December 17 2013 at 9:00 AMWebinarInformed consent is a paramount part of ethical human participant research. Learn about the required and optional elements in an informed consent document, the circumstances when the consent process and documentation can be altered or waived, and other consent options used in research. When: Tuesday December 17, 9:00 am – 10:00 am Where: Your Desk, Link to access webinar will be sent upon registration. Speaker: Ray-Nitra Pugh, Education Coordinator, IRB Administration Office
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