Facility & Location Overview

Agile Clinical Research Trials (ACRT) is strategically located in the heart of Atlanta’s healthcare corridor, providing convenient access to diverse patient populations, major healthcare systems, and transportation networks. Our location supports efficient study execution, participant accessibility, and rapid access to emergency medical services when needed.

The site operates from an independent 4,200-square-foot clinical research facility designed specifically to support clinical trial operations. The facility includes:

• Patient-Centered Care – Our staff actively engage with and support participants to ensure a positive study experience while delivering high-quality clinical outcomes.
• Five fully equipped examination rooms
• Spacious patient reception and waiting area
• Dedicated clinical research workspaces
• Secure study document and investigational product storage areas
• High-speed internet connectivity
• Fully digital clinical research infrastructure
• Private consultation and study coordination areas

Our facility is conveniently located at the intersection of Interstate 285 and Georgia State Route 400, providing easy access for study participants, sponsors, monitors, and CRO personnel.

Transportation & Accessibility

• Located directly on a MARTA bus route
• Approximately 1 mile from a MARTA rail station
• Easily accessible from major Atlanta metropolitan areas
• Approximately 22 miles from Hartsfield-Jackson Atlanta International Airport
• Convenient access for local and regional study participants

Healthcare Network Access

ACRT is located near several major hospitals, emergency departments, specialty physician practices, and healthcare providers, providing rapid access to medical support and referral networks. Multiple hospital systems and emergency care facilities are located within a short distance of the site, supporting participant safety and specialty care needs.

Digital Research Environment

As a 100% digital clinical research site, ACRT utilizes fully integrated 21 CFR Part 11 compliant electronic systems throughout the clinical trial lifecycle. This digital infrastructure supports:

• Electronic source documentation (eSource)
• Electronic regulatory management
• Remote monitoring capabilities
• Real-time study visibility
• Secure electronic document management
• Enhanced data quality and compliance
• Efficient sponsor and CRO collaboration

Equipment & Calibration

All clinical research equipment is maintained in accordance with established quality procedures and is calibrated annually, or as required by manufacturer specifications and study protocols. Calibration records and maintenance documentation are maintained and available for sponsor review.

Our facility is equipped to support a broad range of clinical trials and study procedures, ensuring a high standard of quality, safety, and regulatory compliance.

Suggested Equipment Section

After the paragraph “Site has onsite calibrated equipment as follows,” you can list:

• Digital Weight Scale
• Stadiometer (Height Measurement)
• Vital Signs Monitor
• Blood Pressure Monitors
• Pulse Oximeters
• ECG/EKG Machine
• Spirometer
• Centrifuge
• Refrigerators (2°C–8°C)
• Freezers (-20°C)
• Ultra-Low Freezers (-70°C / -80°C, if available)
• Temperature Monitoring System
• Phlebotomy Equipment
• Crash Cart
• AED (Automated External Defibrillator)
• Examination Tables
• Laboratory Processing Area
• Secure Investigational Product Storage
• Backup Power Supply

Off Site

• MRI / MRE
• PET
• Ultrasound
• X-ray
• DXA Scan
• Overnight stay
• Mammogram
• GMP Lab for Cell Therapy