IRB Services
Finally... an IRB that focuses exclusively on natural products research
To comply with FDA regulations, all research projects involving human participants, regardless of the type of research conducted, must be reviewed and approved by an IRB (Institutional Review Board) before recruitment begins. Most research projects will require ongoing IRB oversight throughout the study.
Expedited Review
Most natural product studies fall under the federally defined category of "expedited review." NRI can access your study, suggest adjustments to help it achieve the "minimal risk" criterion, and provide approval and ongoing oversight.
Annual Review
All studies lasting more than one year are required to undergo annual continuing review. NRI's procedures for continuing oversight makes this process straightforward.
Exempt Determinations
While all studies must undergo initial IRB review, federal regulations do allow certain types of studies to be exempt from ongoing oversight. Our IRB can assess your study and make a determination of exemption in as little as 2-3 business days.
Contact
For more information on our IRB services, our current board membership, or our current price list, fill out the form below: