OUR HIGHLY QUALIFIED TEAM OF MEDICAL AND RESEARCH DOCTORS, EXPERIENCED COORDINATORS, AND HIGHLY TRAINED STAFF MEMBERS ALL PLACE OUR PATIENTS’ SAFETY AND COMPLIANCE AS OUR TOP PRIORITY.

We are a research site  with 12 full-time research staff members who are completely dedicated and trained to conduct clinical trials. Our study coordinators are Certified Clinical Research Coordinators, GCP trained and IATA certified.  We also have a dedicated regulatory specialist to oversee all regulatory documentation requirements and submissions as well as contract and budget staff. Our QA teams closely monitor all activity to ensure that our sites are in compliance with internal and protocol SOPs and regulations. Our qualified staff provides the ability to rapidly contract, obtain IRB approvals, and launch new trials, typically within a matter of days.

- Four patient exam rooms

- CLIA Certified Clinical Laboratory

- Large conference room

- Dedicated coordinator room

- Private office with three workstations specifically designated and equipped for pharmaceutical company sponsor and/or monitor use

- Spacious waiting room with TV lounge for subjects with comfortable seating.

- Ample storage space for confidential patient records and sensitive clinical trial information.

- All study drug is kept in a secure locked medication room

- 24/7 monitored security cameras

- Storage is kept locked at all times and is only accessible to assigned clinical personnel. Limited access is strictly enforced.

- Refrigerators, -20 & -80°C Freezers

- 24/7 Electronic Temperature Monitoring System with Min and Max temperature recording

- Refrigerated and standard centrifuges

- ECG machines

- Backup generator in case of power failure

- High speed wireless internet access throughout

We cordially invite our sponsors and potential customers to get in contact with us in order to schedule a walk-through tour of our facilities.