Our Mission is Simple. At New England IRB, our priority is to ensure the rights and welfare of human subjects in research, and we are committed to an ethical and thorough review process. We are an AAHRPP-Accredited organization reviewing:

All phases of FDA-regulated drug, biologic, and device studies
Patient-reported outcomes studies
Registry studies
Peri-approval and post-approval studies
Socio-behavioral and educational studies
Requests for Exemption
“What distinguishes New England IRB from others is the customer service.
I have one person I call upon for all questions, instead of an anonymous entity.”
– Regulatory Specialist
“It’s no secret that your IRB is an outstanding professional organization,
not to mention the staff at New England IRB is great to work with.”
– Clinical Research Manager, Sponsor
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