We are a dedicated clinical trial site with direct access to a large, ethnically diverse, family-medicine patient database. We take seriously the safety of patients that are enrolled in the study that we participate in and we diligently follow clinical protocols to ensure that each clinical trial we partake in is conducted per protocol and ICH-GCP guidelines. The clinics we are affiliated with are well established, having been in practice for average of 10 years, so we have access to private database for targeted subject recruitment purposes. The Principal Investigator and Sub-Investigators are all licensed medical Doctors with research experience as well as the rest of the site staff. Our research team all have several years of experience and in-depth knowledge of clinical research and clinical site responsibilities. We also work with subject recruitment services, e.g., Acurian, e-patient finder etc. based on Sponsor or CRO recommendation.
We have a dedicated clinical research team, as well as all of the necessary components to conduct clinical trials according to FDA regulations, ICH/GCP guidelines, Sponsor’s Protocol and IRB guidelines. We are equipped with consenting room, monitoring rooms, double locked access controlled temperature monitored drug room/drug cabinets, locked and temperature monitored drug refrigerator, locked and temperature monitored -20 degree and -70 degree freezers, locked cabinets for subject charts/study regulatory binders/lab supplies, CLIA waived lab, annually calibrated research equipment (centrifuge, weight scale, sphygmomanometer, min/max thermometers). Our staffs are IATA certified, GCP certified, HIPAA trained and CCRP certified. Our staffs are proficient in using different EDC systems, IVRS and other study management portals. The site has access to dry ice and located across from one of Georgia’s biggest hospital network (Wellstar Hospital).