Sorry, you need to enable JavaScript to visit this website.

Site-wide links

IRB Forms

 On January 21, 2019 the Final Rule to update the current regulations at 45 CFR 46, Subpart A - "Federal Policy for the Protection of Human Subjects" (the Common Rule) will be effective.
Substantive revisions were made to the regulations to “modernize, strengthen, and make more effective” (HHS 2017) the current system of oversight that has been the federal Common Rule since 1991. The revisions are intended to:

  • Better protect human subjects involved in research
  • Facilitate research
  • Remove ambiguity
  • Reduce regulatory burden

Information about the modifications can be found on the OHRP website. CITI Program also has a module on the Revised Common Rule .
 Impact on Researchers

  1. Increased number of research categories approved under Exempt review
  2. Continuing review no longer necessary for most non-exempt research activities
  3. New Consent Process requirements

The RIT review process will continue as it is currently with some modifications to existing forms and some researchers may be required to submit additional information.  The updated HSRO website will be online January 21, 2019 and the HSRO will assist researchers with the transition during the next few months.
NTID Form A - Use if your research question focuses on Deaf and Hard of Hearing populations.
 
External researchers (those not affiliated with RIT/NTID) conducting research on questions related to Deaf and Hard of Hearing populations can use NTID Form A for external researchers.
 
RIT Form A - Use if your research question is not related to Deaf and Hard of Hearing populations. Both RIT and External researchers can use this form.