Announcements

ORI/IRB Listened: Streamlining E-IRB Application Process

Since E-IRB has been put into production, ORI has received feedback indicating preparation of the application by study support-staff is cumbersome due to the multiple points at which the Principal Investigator (PI) is required to log-in to E-IRB and perform a PI-only task.

April IRB Review Newsletter

Consent Language for Certificates of Confidentiality (CoC) Automatically Issued as a result of the NIH CoC Policy Change

What is Informed Consent? From Perception to Process

The Office of Research Integrity and Center for Clinical and Translational Science will be providing a hands on workshop on informed consent regulatory requirements.

January 22, 2018 Transition to E-IRB

Effective January 22, 2018, new Expedited and Full Review Applications must be submitted via the new web-based application system, "E-IRB".

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