IRB Policies and Procedures

Human Research Protection Program

Introduction

The University of Illinois at Springfield Institutional Review Board (IRB) operates under policies and procedures mandated by the U.S. Department of Health and Human Services and the Office for Human Research Protections. These policies are available for review at the Office for Human Research Protections. (Update: The federal “Common Rule” was revised on 19 January 2017 and effective 21 January 2019.

Elements of Informed Consent

Regulations now require that federally-sponsored research projects contain a concise and focused presentation of the key information that is most likely to help potential subjects understand why they might or might not want to participate in the study. The key information must be presented first and must include the following:

Responsible Conduct of Research

Research Ethics Training at UIS

The ethical conduct of research is critical to modern society.  Unfortunately, there are examples of unethical practices by professionals and students.  The purpose of our program is to educate our students on the various aspects of responsible research.

Research involving human subjects is regulated by federal laws and NIH and NSF grant recipients are required to have a research ethics training program in place.

IRB and Integrity Programs

UIS is committed to research integrity. The Office of Research & Sponsored Programs provides resources to assist faculty, staff, and student researchers affiliated with the University of Illinois Springfield with meeting research compliance requirements.

Boards and committees providing research oversight at UIS include the following: