An institutional review board (IRB), also known as an independent ethics committee (IEC), ethical review board (ERB), or research ethics board (REB), is a committee at an institution that applies research ethics by reviewing the methods proposed for research involving human subjects, to ensure that the projects are ethical. The main goal of IRB ...

What is an Institutional Review Board (IRB)? Under FDA regulations, an IRB is an appropriately constituted group that has been formally designated to review and monitor biomedical research ...

Jun 28, 2021 · Institutional Review Boards, or IRBs, review research studies to ensure that they comply with applicable regulations, meet commonly accepted ethical standards, follow institutional policies, and adequately protect research participants.

Feb 24, 2024 · The institutional review board (IRB) is a research ethics committee that reviews and approves research involving human subjects. The IRB’s primary responsibility is to protect the rights and welfare of research participants.

Institutional review boards (IRBs) or research ethics committees provide a core protection for human research participants through advance and periodic independent review of the ethical acceptability of proposals for human research.

An institutional review board (IRB) is the institutional entity charged with providing ethical and regulatory oversight of research involving human subjects, typically at the site of the research study.

Dec 18, 2024 · Institutional review board (IRB), in the United States, ethics committee that reviews proposed and ongoing research involving human subjects. The institutional review board (IRB) exists to protect the rights and safety of human subjects who participate in research studies.

Jan 17, 2023 · Institutional Review Boards (IRBs) assess the ethics and safety of research studies involving human subjects, such as behavioral studies or clinical trials for new drugs or medical devices.

An Institutional Review Board (IRB) is a committee set up by an organization to review, approve, and regulate research conducted by its members, on its premises, or under its sponsorship (Babie, 2001).

Clinical trial procedures are reviewed by institutional review boards (IRBs). These boards are composed of at least five members that include scientists, doctors, and lay people.