Do YOU need the IRB*?

If you answered YES to any of these questions - YOU DO NEED THE IRB.

 

 

All research projects using human subjects, classroom assignments as well as individual research, must be submitted to the IRB for review.  No phase of a project may begin until IRB approval is obtained.

Form A applications may be submitted to the Office of Research Services (ORS) any time.  Form B and C applications must be reviewed at a full IRB meeting and must be received no later than 10 days preceding a meeting.

Meeting Schedule

September 20 December 20 March 21
October 25 January 17 April 25
November 15 February 21 May 16

(Summer meetings will be scheduled as needed.)

 Note: If your department has a Departmental Review Board (DRB), contact your department chair for procedures.

*Institutional Review Board for the Protection of Human Subjects
Established in response to federal mandates resulting from the 1979 “Belmont Report” (Ethical Principles and Guidelines for the Protection of Human Subjects of Research) of the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research.  The federal regulations are “Title 45, Code of Federal Regulations, Part 46.”  Links to both documents may be found on the ORS website.


Office of Research Services (ORS), O’Hara 224, 941-6180
Eileen Callahan, Director of Research Services/IRB Administrator
callahane1@scranton.edu

 


The ORS Website was created and is maintained by Maria C. Landis.
E-mail
LandisM2@scranton.edu with content questions and/or concerns.
Updated August 2005