We are proud to serve as a strong partner to the clinical research community. Throughout our history, our research has included oversight in:

  • All phases of FDA-regulated, drug, biologic, and device studies
  • Expertise reviewing Phase I studies
  • Multisite / multicenter studies
  • Single site studies
  • Review spanning a wealth of therapeutic areas

To aid in the research that we review, our advisors and review Board members include the leading experts in every major clinical specialty, enabling us to provide highly specialized review services in the therapeutic areas and phases to which most research funding is directed.

Midlands IRB will bring this comprehensive experience to bear on your research; this experience will translate into ethical oversight that improves the quality of the research you conduct has positive impact on the lives you touch.