If you are working on a government-funded research study, the regulations you will be required to follow come from the: Nuremberg Code National Institute of Health ( NIH) US Department of Health and Human Services (DHHS). Bioresearch Monitoring Program (BIMO) Question 13 ( 2 points) The FDA considers advertising to be a part of the informed consent process. An IRB is expected to review all research advertising materials. True False.