Welcome to the 2013-2014 school year and especially to the Class of 2017. The Board will convene again starting September, 2013. The 2013-2014 academic year meeting schedule has been posted. Please adhere to all deadlines for full review projects.
The IRB has a new submission e-mail address. All submissions should be sent to: email@example.com. Please ensure to update your address books.
NEW Human Research Protection Web-based Training
FDU has licensed the Collaborative Institution Training Initiative (CITI) program for web-based training in human research subject protection, responsible conduct of research, animal care & use, and export control. The training and information may be accessed here: http://view.fdu.edu/default.aspx?id=5825.
Please note the NIH Human Research Subject Protection Training will no longer be accepted. Training expires in three (3) years from the date of last completion. If you need to update your training, please complete CITI as required. If you have any questions, please contact 201-692-2219.
NEW Forms Posted
New and revised IRB Application forms can be found NOW at "IRB Forms, Templates and Guidance Documents". Please note that the IRB will no longer acccept proposals using old forms.
Please check this site periodically for announcements, updates and form revisions. Feel free to contact the IRB Human Research Compliance Manager with any questions.
The Institutional Review Board (IRB) at Fairleigh Dickinson University (FDU) was created to ensure and enhance the protection of the rights and welfare of human research subjects as well as enhance the education of students, faculty and staff about their ethical responsibility to protect research participants. All research involving human subjects are reviewed prior to initiation and at continuing intervals as required in the regulations, to ensure compliance with all ethical, professional, community, federal and state standards. The procedures and regulations followed by the IRB are in compliance with the Office of Human Research Protection (OHRP) of the Department of Health and Human Services (DHHS). In regards to the review and conduct of research, actions by the Board will be performed in accordance with the ethical principles highlighted in The Belmont Report and DHHS policies and regulations at 45 CFR 46. Actions will also conform to all other applicable federal, state, local laws and regulations.
The Board is authorized to and responsible for the review of each research project to determine: (1) approval of human subjects research according to federal regulations; 2) ethical principles identified in the Belmont Report (Respect for Persons, Beneficence and Justice) will not be violated by the experimental procedures; 3) that all subjects will be fully informed of any physical, legal, psychological, or financial risks they may incur, and 4) that the subjects and/or parents/legal guardians freely consent and/or assent prior to participation. The existence of the IRB is a condition with which the University must comply to accept federal funding, including student financial aid, scholarships, and research grants. No research project using human subjects may be undertaken without the Board’s prior approval.
Kim Diccianni, CIP William Pat Schuber, JD
IRB Compliance Manager
Becton Hall, Room 200
1000 River Road
1000 River Road
Kim Diccianni, CIP
William Pat Schuber, JD