Pharmaceutical Study Experience
With years of experience conducting clinical research trials, the Medical Research Group of Central Florida provides pharmaceutical study sponsors the high-quality, efficient data collection needed for FDA approval. Together, our certified Research Coordinators, Investigators and sponsors help develop better medications and treatments for patients around the world.
Conveniently located between Orlando and Daytona Beach, both of our research facilities conduct Phase II, III and IV clinical research studies and fulfill enrollment goals to produce quality data collection. Our participants receive optimal patient care supervised by our Certified Principal Investigator and Board Certified Psychiatrist, Dr. Adly Thebaud and board certified Family Physician Dr. Josette Romain. See the variety of Sponsors, Clinical Research Organizations (CRO) and Institutional Review Boards (IRB) we work with below.
Clinical Trial Participant Demographics
The Expertise and Capabilities Pharmaceutical Study Sponsors Look For
With years of national and international experience delivering efficient, high-quality data collection, Medical Research Group of Central Florida earned the distinction as a trusted medical research facility. Our high integrity and disciplined process management and data collection, complemented with our unique speed to market and expansive patient recruiting team, ensures our sponsors receive the highest value for their clinical research investments.
Trust Medical Research Group of Central Florida to deliver high quality, precise data collection and recruitment. It’s easier than ever to see our facility and meet out team in person. Schedule a pre-site visit to our clinical studies facility conveniently online, today.