Division of Research

Institutional Review Board (IRB)

The Institutional Review Board (IRB) is a committee charged with protecting the rights and welfare of individuals who participate in research.

The IRB reviews research involving human participants to ensure that it is conducted ethically, responsibly, and in compliance with federal regulations, institutional policies, and ethical standards. By balancing the advancement of knowledge with the protection of participants, the IRB plays a critical role in supporting high-quality research and maintaining public trust.

The Brown University IRB reviews research studies conducted at Brown University and at affiliated organizations within Brown University Health and Care New England.

IRB Meeting Schedule

The meeting dates and deadlines below apply only to research that may be greater than minimal risk and requires review by the full, convened IRB, or other situations as guided by HRPP staff (for example, policy exception requests). Unless otherwise instructed by the HRPP team, these dates and deadlines do not apply to minimal risk research, which is reviewed by HRPP staff and the IRB on a rolling basis and does not have submission deadlines.

Transition Period

Please note that during this transitional period, Panel 1 will operate in Huron, while Panels 2, 3, and 4 will operate in IRBNet. Researchers should continue submitting materials in the system they are currently using.

Accordingly, active studies managed in IRBNet may be reviewed by Panels 2–4, while active studies managed in Huron will be reviewed by Panel 1 only, until all IRB panels transition to operating fully within Huron IRB. New projects are eligible to be reviewed by any of the four panels.

For more information about this transitional phase, see the HRPP alignment page.

2026 Meeting Dates

Panel 1Panel 2Panel 3Panel 4
Jan. 8Jan. 14Jan. 21Jan. 29
Feb. 5Feb. 11Feb. 18Feb. 26
March 5March 11March 18March 26
April 2April 8April 15April 23
May 7May 13May 20May 28
June 4June 10June 17June 25
July 2July 8July 15July 23
Aug. 6Aug. 12Aug. 19Aug. 27
Sept. 3Sept. 9Sept. 16Sept. 24
Oct. 1Oct. 14Oct. 21Oct. 29
Nov. 5Nov. 11Nov. 18Nov. 25
Dec. 3Dec. 9Dec. 16 

To ensure sufficient time for review, IRB meeting agendas close two meetings prior to the scheduled meeting date. Complete submissions received at least two weeks before the meeting date are eligible for review. Please note that submissions must be deemed complete by HRPP staff to be placed on the agenda. The HRPP reserves the right to adjust meeting agendas as needed based on submission volume and the variety of submission types.

Return to HRPP Alignment page

Related Pages

The Brown Human Research Protection Program (HRPP) is designed to protect the rights, safety, and well-being of people who take part in Human Subjects Research at Brown. This includes making sure participants understand what they’re agreeing to, keeping their information private, and reviewing studies to ensure they are ethical and fair.
Federal regulations require that all research involving human participants be reviewed and conducted in compliance with guidelines designed to protect their rights and welfare.Determining whether or not a project meets that definition of “human subjects research” is a two-step process.
Research Integrity is a group of teams — including Animal Research Compliance, Export Controls, the Human Research Protection Program, Quality Assurance and Quality Improvement, Conflict of Interest and Regulatory Compliance — that partner with the research community to facilitate ethical research guided by governing policies and regulations.

Contact the IRB

Brown investigators can contact the IRB at 401-863-3050 or irb@brown.edu.