Our staff is GCP, IATA, and CCRP certified. We have a team of investigators, nurses, and other research support staff. Our average startup process takes less than 2 months. We have a robust recruitment process to assure enrollment of subjects in the appropriate clinical trials. We are committed to providing quality research.
Site Diversity Profile:
Diversity of study subject plays an important role. Inclusion of wide patient populations from various, races, ethnic groups, sex, genders, ages help provide evidence that the study product or device will be safe and effective and generalizable in the wider target patient pool if the drug or device is approved.
Site Start-up Timeline: