All human research in which University or affiliate faculty or staff are engaged must be approved or acknowledged by the University Research Integrity or IRB. The University allows certain categories ...

The purpose of this announcement is to provide you with the Human Research Protection Program (HRPP) plans to implement the revised regulations governing research involving human subjects, the Common ...

The U.S. Department of Health and Human Services (“HHS”) and fifteen other Federal Departments and Agencies have announced a proposal to update the Federal Policy for the Protection of Human Subjects ...

A substantial revision to the federal policies mandating the protection of human subjects (Common Rule) took place in January 2019. Of particular interest to researchers is a broadening of the Exempt ...

The full Case Western Reserve University Institutional Review Board (IRB) meets once per month. Meeting dates and deadlines can be found here. An investigator should expect a protocol requiring full ...

The purpose of this SOP is to set forth the procedures to be followed in the initial review of human subjects research protocol submitted to the Brandeis University Institutional Review Board for ...

The IRB/Research Integrity & Security Quality Improvement Program (QIP) serves to improve human research protections. One of the primary quality improvement activities is the internal assessment ...

If so, then you will need to have your research reviewed by the William & Mary Institutional Review Board (IRB) before you begin your research involving human subjects, so that we're sure that your ...

SODM research projects involving human subjects are required to obtain IRB approval from a "home" institution (CWRU or UH) before the start of any research activities. Use the information below to ...

Beginning February 1, 2023, the Cal Lutheran IRB will begin to use the web-based product Cayuse Human Ethics for managing human subjects research studies. Cayuse Human Ethics is an electronic protocol ...

An Investigational Device Exemption (IDE) allows an investigational device to be used in a clinical study in order to collect safety and effectiveness data required to support a Premarket Approval ...

When Brandeis University investigators collaborate with non-Brandeis US investigators, the Brandeis IRB will often enter into a reliance agreement with either the collaborating investigator’s ...