IRBs

The U.S. federal government is preparing to launch a set of sweeping new regulations that will have a major impact on how biomedical researchers and social scientists work. It will require researchers to change how they get ethics approval, how they collect informed consent from participants, and more. Read More

Julie Ozier, MHL, has been named director of Vanderbilt’s Human Research Protection Program (HRPP) and Institutional Review Board (IRB). Ozier has worked with the HRPP and IRB for 11 years, has been associate director since 2007, and at Vanderbilt since 1996. Read More

Failing to get proper consent from parents in a study that potentially put babies at risk is unquestionably a regulatory failure and perhaps a moral failure, according to Laura Stark, an expert on medical regulation and ethics. Read More