The primary function of the the Independent Investigational Review Board, Inc. [IIRB] is to protect the rights and welfare of human subjects involved in clinical investigations. IIRB activities are conducted in accordance with the Food and Drug Administration regulations, and the Department of Health & Human Services.

Simplicity
Our streamlined procedures and personalized service makes it easy for you to be in compliance with the regulations protecting the rights of volunteers enrolled in a research study.

Timeliness
We know that when you have a final research protocol, you are ready for the IRB approval letter and stamped informed consent document. We eliminate IRB delays through teamwork and efficiency.

Compliance
We believe that compliance with the regulations begins with our commitment to the protection of the rights and welfare of the research volunteer and includes thorough knowledge of regulatory requirements.