Dr. Brody is considered a thought leader in the field, is often consulted regarding study design and feasibility, and serves on Advisory Boards for several pharmaceutical companies. The principal and sub-investigators are on-site full-time supervising all trial activities. BMR has an extensive patient database, as well as a history of collaboration with community physicians to bring research opportunities to their patients. Our professional, full-time, ACRP certified study staff are re-certified annually on GCP and ICH guidelines, and work hand-in-hand with our investigators to ensure rapid data entry and expedited query responses. Our center utilizes central IRBs, and can turn around regulatory documents and contracts/budgets within 24 hours, ensuring an expeditious study start-up. Full staff certified annually in GCP, ICH, OSHA, HIPAA, and PHI. Clinical research coordinators are ACRP certified. Principal investigator is CPI (Certified Physician Investigator) by ACRP.