The Belmont Report serves as the ethical basis upon which regulations on the use of human subjects in research are based. These principles do not technically govern the research process, and yet are essential to ensure that research is done ethically. At the 2014 Advancing Ethical Research Conference, Gigi McMillan interviewed Ilene Wilets, PhD, CIP, executive director of the institutional review board (IRB) at the New York State Psychiatric Institute, for People and Perspectives. During her interview, Dr. Wilets explained, “you have to have the ethical underpinnings woven into the fabric of human subjects protections.”
In order to get a better understanding of how the Belmont Report is being applied to functioning IRBs, Ms. McMillan asked Dr. Wilets, “How do you see the principles of the Belmont Report being applied in the actual IRB process?”
Respect for Persons: The Belmont Report states, “Respect for persons requires that subjects, to the degree that they are capable, be given the opportunity to choose what shall or shall not happen to them. This opportunity is provided when adequate standards for informed consent are satisfied.” In thinking about her own IRB office, Dr. Wilets spoke of developing a process that leads to valid, informed consent. Further, she also emphasized that we should not compare informed consent as it exists in research to other times when someone may consent to doing something – having Italian food for dinner, or going to a movie, for instance.
Beneficence: In terms of beneficence, the Belmont Report offers, “Two general rules have been formulated as complementary expressions of beneficent actions: (1) do not harm and (2) maximize possible benefits and minimize possible harms.”
The views, opinions and positions expressed by these authors and blogs are theirs and do not necessarily represent that of the Bioethics Research Library and Kennedy Institute of Ethics or Georgetown University.