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Welcome

The Human Subjects Office (HSO) was established by the Vice President for Research to provide administrative support for the University of Iowa Institutional Review Boards. An Institutional Review Board is a group of individuals charged with reviewing proposed research involving human subjects to ensure the protection of those subjects and compliance with federal human subjects regulations. The University of Iowa has three such review boards, each consisting of faculty, staff, and representatives from the Iowa City community.

Mission

The mission of the University of Iowa Institutional Review Boards is to assure that the rights and welfare of human subjects are adequately protected in research.

Upcoming Events

Wed, Apr 22, 2015 - 2:00pm to 4:00pm

Office Hours Wednesday Spring 2015 - Location: 101 Hardin Library

Thu, Apr 23, 2015 - 10:00am to 12:00pm

Office Hours Thursday Spring 2015 - Location: 101 Hardin Library

Mon, Apr 27, 2015 - 2:00pm to 4:00pm

Office Hours EASTSIDE - Location: 304 Lindquist Center - Paul Blommers Measurement Resources Library

Upcoming Meetings

Wed, Apr 22, 2015 - 9:00am to 12:00pm

IRB 02 Full Board Meeting - Location: 101 HLHS

Thu, Apr 23, 2015 - 2:00pm to 5:00pm

IRB-01 Full Board Meeting - Location: 101 HLHS

Announcements

Changes to Question VI.13 of the HawkIRB application

There has been a wording change to VI.13.  The question has added a new bullet to address the enrollment of non veterans under IRB-03 studies.  However, all IRB (01,02,03) applications will see this update even though they may not indicate IRB-03 in I.1.  The question reads the following:  VI.13 Describe EACH of your subject populations

FDA Webinar April 20: Draft Guidance for Industry: Use of an Electronic Informed Consent in Clinical Investigations: Questions and Answers

On Monday, April 20, 2015, from 1:00 p.m. – 2:00 p.m. EDT, the Office of Medical Policy (OMP) in FDA’s Center for Drug Evaluation and Research (CDER) will present a webinar on the draft guidance for industry, Use of an Electronic Informed Consent in Clinical Investigations: Questions and Answers.

Human Subjects Research: Current Challenges in the Modern Research World

We are delighted to announce                               The Office for Human Research Protections (OHRP) Research                                                              Community Forum                                            Co-hosted with Governors State University, Illinois “Human Subjects Research: Current Challenges in the Modern Research World”
Tuesday, July 28, 2015, 7:00 a.m. to 5:00 p.m.
Governors State University
​One University Parkway,
University Park, IL 60484

One-Day Joint OHRP and NIH Workshop on Human Research Protections

We are delighted to announce a one-day workshop on human research protections jointly organized by the HHS Office for Human Research Protections (OHRP) and the Office of Extramural Research (OER) of the National Institutes of Health (NIH) entitled              “Getting through Human Research Reviews without Pain”                                   Wednesday May 6, 2015, 9 a.m. to 4 p.m.                                   Renaissance Baltimore Harborplace Hotel                               202 East Pratt Street, Baltimore, Maryland 21202

Did you know we have an FAQ for questions we frequently are asked

Follow the link found here and click on the category title for a list of  frequently asked questions pertaining to that topic.   Please check out the New Revised Guidelines & FAQ regarding Research Payment and Compensation.