Our streamlined and thorough planning, coordination, and execution process ensure both efficiency and quality. We have the following capabilities:

• Full-time on-site physician investigator

• Certified clinical research coordinators

• Veeva Site-Vault for e-reg binder management

• Use of central Institutional Review Board

• On-site accommodation for pre-study, initiation, routine, and close-out monitoring visits

• Comprehensive subject recruitment and enrollment tracking

• Maintenance of source documents and timely data entry

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Each of our facilities include the following capabilities:

 • Patient Waiting/Check-in Area

• 5 Clinic Examination Rooms

• Lab/phlebotomy room

• Multi-purpose conference room for SIVs, Investigator meetings, trainings, etc

• Principal Investigator Office

• Study Coordinator Office

• Monitor/CRA Room

• Specified private client monitoring area with WIFI

• EKG Machines

• Secured Storage Room for Subject Binders and IP/Shipping Supplies

• EMR

• E-Consent Capability

• Veeva Site Vault Profile for eRegulatory Binders

• Laboratory freezers (-70C and -20C)

• Refrigerated and Non-refrigerated Centrifuge

• Printer, Scanner, and Fax Machines

• LCD Screens in the waiting area and every room with capability of presenting advertisements for trials and health education.