At Community Research, we know that cost and timelines are critical concerns. Our infrastructure is designed around separate, dedicated departments that help ensure your trials not only have enough of the right kinds of subjects, but that the other vital facets of the trial process are also dealt with in a timely, professional manner. In order to facilitate that goal and to allow our Investigators and Coordinators to stay focused on quality subject care, we have a separate Regulatory Department, staffed with a diverse group of professionals with over 20 years of combined regulatory experience, handling all the necessary regulatory paperwork for sponsor, CRO and IRB submissions.

Furthermore, for maximum efficiency and timely approvals, we always work with Central Institutional Review Boards. And because of our unique infrastructure, we can easily work with any Central IRB of your choosing.