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University of IowaHuman Subjects Office / IRB

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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.

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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.

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Wed, Aug 05, 2024 - 2:00pm to 4:00pm

IRB Office Hours via Zoom - Location: Zoom: http://uiowa.zoom.us/j/93606863003

Wed, Aug 12, 2024 - 2:00pm to 4:00pm

IRB Office Hours via Zoom - Location: Zoom: http://uiowa.zoom.us/j/93606863003

Wed, Aug 19, 2024 - 2:00pm to 4:00pm

IRB Office Hours via Zoom - Location: Zoom: http://uiowa.zoom.us/j/93606863003

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Mon, Aug 03, 2024 - 熊猫加速器怎么使用 to 5:00pm

IRB-01 Meeting (Click for more dates) - Location: 101 HLHS

Thu, Aug 06, 2024 - 熊猫加速器怎么使用 to 5:00pm

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New IRB Connection Newsletter

The July 2024 edition of our IRB Connection newsletter is now available.

Read More...

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Guide for Human Subjects Research
UI IRB SOP
Certification in Human Subjects Protections (CITI)
WIRB
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Failure to publish trial results exposes patients to risks without providing benefits

Science Daily
How electronic health records can benefit clinical trials

Science Daily
FDA Drafts Guidance on Scientific and Ethical Considerations in Including Pregnant Women in Clinical Trials

Regulatory Focus
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The Hill

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HHS and 16 Other Federal Departments and Agencies Issue a Final Rule to Delay for an Additional 6 Months the General Compliance Date of Revisions to the Common Rule While Allowing the Use of Three Burden-Reducing Provisions during the Delay Period
HHS and 16 Other Federal Departments and Agencies Announce a Notice of Proposed Rulemaking Proposing to Delay for an Additional 6 Months the General Compliance Date of the Revisions to the Common Rule

FDA News

FDA Draft Guidance on "Pregnant Women: Scientific and Ethical Considerations for Inclusion in Clinical Trials"
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NIH Notices

Use of a Single Institutional Review Board for Multi-Site Research
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