August 2023


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The IRB Review

A compilation of information, announcements, & updates for UK Institutional Review Board (IRB) members, research investigators, & others involved with human subject research.

Summer Refreshments

ORI recommendations for summer training "refreshments" include the OHRP Respecting Persons webinar and the CITI Artificial Intelligence (AI) and Human Subject Protection webinar. Both are linked below.

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Click to View*

*The AI and Human Subject Protection webinar must be added as an optional CITI course to access. Instructions for adding an optional CITI course are here:

Add CITI Course Instructions

REGISTRATION OPENING SOON!

Virtual Regional Conference

November 2-3

12:00 - 4:00 pm ET


Join us November 2-3 for our annual human research protections conference, entitled "Human Research Protections: Unstoppable". This year's event will address issues of critical importance to human research protections, including:


  • Artificial Intelligence
  • Diversity, Equity, & Inclusion
  • Human Research Protection Hot Topics


Questions? Please email orcraeducation@cchmc.org and

reference the Human Research Protections Conference.

Test Your IRB Knowledge:


Can a protocol application be submitted if a survey, questionnaire, or interview instrument has not been developed at the time of initial submission? 

***Keep Reading for the Answer***

Upcoming ORI Office Hours

Thursday, August 17, 12:30 pm - 1:30 pm

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Click Here for All Office Hours Dates/Times

The Office of Research Integrity offers consultations by phone, Zoom, or in-person. Consultations are offered for studies in development (with or without an E-IRB submission) as well as approved research projects.

Click Here to Request a Consult

Answer to the Trivia Question:


Yes. A protocol application can be submitted and provisionally approved without a final instrument attached. However, researchers should describe the nature of the survey-questionnaire-interview and the procedures for developing the data collection instrument in the research description of the protocol application. 



Once the survey instrument is developed it will need to be submitted as a modification request (MR) to the IRB for approval prior to implementation. Investigators may not initiate any changes in the research without prior IRB review and approval, except where necessary to eliminate apparent immediate hazards to the subject.