IRB Approval is confusing enough, we’ll guide you
through the entire process.
Personalized Researcher
Support For IRB Approval

How Can We Help?

We demonstrate our commitment to our clients everyday. This is why more than 90% of our clients submit more than one study.
Because our reviewers are also researchers, we often make optional suggestions to save you time and money.



Submitting a study to Solutions IRB was a professional and pleasant experience. The staff handled everything and pointed out things that I was missing right at the start. I felt very comfortable with them and confident that my submission would be accepted. It was a learning experience that I will not soon forget. Thank you for taking the time to thoroughly explain the process and offer suggestions for future projects.


There is often confusion about “exempt review” among researchers, and this is entirely understandable. Sometimes we are asked: “well, I’ve already determined that this is an exempt study—so why do I need an IRB to do a review?” Projects that

Generally, Institutional Review Boards (IRBs) require investigators clearly and accurately inform human subjects about research during the recruitment and consent process. Human subjects are defined as a living individual about whom an investigator conducting research obtains (1) Data through intervention

The Common Rule (45 CFR part 46) published in 1991 is used by 15 Federal departments and agencies to provide protections for human subjects involved in research activities. The Common Rule also provides guidelines for the administration of the IRB