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New England IRB has been reviewing Social, Behavioral and Educational Research studies for over 25 years.

After your study is submitted to New England IRB and scheduled for Board review, an IRB Administrator will be assigned to your study. The IRB determination letter will be signed by this individual and the IRB Administrator will remain your IRB contact throughout the course of the study. IRB Administrators are assigned to studies based on the organization submitting the study, so that if your organization has worked with New England IRB in the past, you will continue working with the same Administrator.

Founded in 1988, New England IRB was one of the first central IRBs established to meet the ethical review needs of the clinical trials industry. For studies ranging from one site to several thousand, New England IRB is focused on the protection of human subjects, responsiveness and service.

New England IRB is the premier central IRB, providing quality study review services, merging quick turnaround with ethical support of study participants.

I really enjoy working with NEIRB and the wonderful staff. I cannot say enough positive things about the IRB -- the people, the process, the expertise, and the great working relationship we have established over the years.

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