At CRWI from study feasibility to study closure with Sponsors & CRO’s is what we do well.  Our trained staff is experienced in moving studies from initial phase to final FDA approval/denial.  Our scope of practice is varied, and we are here to help our Sponsor reach every goal and milestone along the research continuum. Solid experience in completing the most challenging studies.  We have a comprehensive database of patients who have research potential with cultural diversity.  Proven track record for regulatory submission, contract approval, and meeting as well as exceeding enrollment goals.