Office of Research Integrity
The UK Office of Research Integrity (ORI) has developed a guidance document outlining plans for transitioning to/overview of the revised human subject regulations (a.k.a., “the Common Rule”).
- Office of Research IntegrityThe transition to the Revised Federal Policy for the Protection of Human Subjects (Common Rule) has forced the Office of Research Integrity (ORI) and Institutional Review Boards (IRB) to issue a Temporary Freeze on New Initial IRB Applications. Any protocol approved prior to January 20, 2019, must comply with the Current Rule and any protocol approved on or after January 21, 2019, must comply with the Revised Rule.
- Office of Research Integrity
Click here to read the IRB Review Newsletter:
- Office of Research IntegrityBased on feedback from researchers, IRB members, and participants from the Informed Consent Workshops, we have made revisions to both the Medical and Nonmedical Informed Consent Template.
- Office of Research IntegrityThe Office of Research Integrity and Center for Clinical and Translational Science will be providing a repeat hands on workshop on informed consent regulatory requirements
- Office of Research Integrity
Click Here to read the IRB Review Newsletter.
- Office of Research Integrity
Starting September 2018, the Nonmedical Institutional Review Board (IRB) will be convening on a monthly basis rather than a triweekly schedule.
- Office of Research IntegrityNIH funded studies that were ongoing or started after December 13, 2016 that collect “identifiable, sensitive information” from subjects, are deemed to have a Certificate of Confidentiality.
- Office of Research IntegrityThe conference provides national level speakers and continuing education credit at a regional venue. The purpose of this conference is to address issues of critical importance to human subject protections.
- Office of Research IntegrityOn May 17, 2018, a "PI Contact Information" feature in high demand by researchers was installed in the E-IRB system.