News

Early results from piloting a new way to manage Institutional Review Board submissions shows an improved turnaround time and increased employee engagement.

A work group was convened to discuss the participation cost language in the consent template, and institution-wide expectations for research participation cost coverage when a research participant is billed for research related activities that will not be covered by the study, sponsor, or insurance.

The HRPP has changed the requirements for certain types of research that use the short form method of consent

Prof. Michael Oakes of the School of Public Health (SPH) was appointed associate vice president for research.

The Board of Regents approved an updated policy for Research Involving Human Participants.

The IRB provided an overview of the revised Common Rule and how to prepare for the regulatory changes in January 2019. Listen to the recording to learn more about the revisions that go into affect on January 21, 2019.

Vice President for Research Allen Levine has appointed Michelle Biros, M.D., to serve as deputy institutional official for biomedical studies for the University of Minnesota’s Institutional Review Board, effective May 1, 2018.

On April 20, 2018, OHRP proposed an additional delay to the Revised Common Rule. If finalized, the Revised Common Rule would require institutions to continue to comply with the requirements of the current Common Rule until January 21, 2019. This would be a six-month delay of the effective and compliance date of July 19, 2018.

See updates to the Toolkit for the month of March.

Protecting research participants is the responsibility of everyone within an organization and is not limited to the Institutional Review Board (IRB). The Human Research Protection Program (HRPP) committee has a mission to collaborate in the development, coordination, and evaluation of the University’s HRPP.