Announcements

September IRB Review Newsletter

Click here to read the IRB Review Newsletter: In this issue:

Updated Informed Consent Templates

Based 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.

Repeat Workshop: What is Informed Consent? From Perception to Process

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

July IRB Review Newsletter

Click Here to read the IRB Review Newsletter. In this issue:

Nonmedical IRB Meeting Schedule Change

Starting September 2018, the Nonmedical Institutional Review Board (IRB) will be convening on a monthly basis rather than a triweekly schedule. The new schedule will provide researchers with more time between submission deadlines to prepare their applications for Full Review. This change will also allow researchers to be more proactive and to contact Office of Research Integrity (ORI) staff for questions or feedback on applications prior to IRB review.

National Institutes of Health (NIH) Certificate of Confidentiality (CoC) and Participant Payment

NIH 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.

20th Annual Human Subject Protection Conference--Registration Now Open

The 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.

E-IRB Improvements for Researchers Continue

On May 17, 2018, a "PI Contact Information" feature in high demand by researchers was installed in the E-IRB system.

Repeat Workshop: What is Informed Consent? From Perception to Process

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

UPDATE: Streamlining E-IRB Application Process

ORI is pleased to announce that the streamlining feature promised in the April 17, 2018 announcement has been put into production sooner than anticipated!

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