Tech
Built for Continuous Observation
Our facility combines flexible clinical space with an integrated video network designed to support continuous observation throughout Phase I studies.
Ceiling-mounted 4K PTZ cameras provide comprehensive coverage of the observation room, while portable PTZ cameras can be positioned wherever additional visibility is required. Each camera can be remotely panned, tilted and zoomed, allowing research teams to adjust their view without entering the participant environment.
This creates a less intrusive observation experience. Participants can move, rest and interact more naturally while authorized study personnel monitor them from the adjoining observation area or another designated location within the facility. Researchers maintain visibility without requiring additional personnel to remain inside the participant space.
One Connected Video Environment
Technology-Enabled Capabilities
- Continuous 24-hour participant observation
- Remotely controlled pan, tilt and zoom camera coverage
- Portable cameras for flexible study configurations
- Scalable network-based camera expansion
- Integration of cameras, computers, mobile devices and imaging sources
- Real-time multiview and picture-in-picture monitoring
- Long-duration and multi-source recording
- Remote observation from other areas of the facility
- Live collaboration and external broadcast capabilities
- Facility-wide video routing to designated displays
A Longitudinal Patient Population of 200,000+
Purpose-Built for Modern
Phase I Research
Traditional trial environments often require physicians, sponsors and research personnel to enter the participant area to observe study activity. Our connected infrastructure allows authorized teams to remain closely engaged while reducing unnecessary traffic and disruption within the trial environment.
The result is a purpose-built Phase I setting that provides researchers with greater visibility, more flexible oversight and centralized access to the video and information needed throughout the study.
Regulatory
Dedicated regulatory specialists coordinate essential study documentation, Central IRB submissions, financial disclosures, Form FDA 1572 documentation and ongoing regulatory requirements.
Patient Recruitment
Dedicated recruiters focus on patient identification, pre-screening, outreach and enrollment support using both data-driven and community-based recruitment strategies.
Research Coordination
Clinical research coordinators focus on protocol execution, patient visits, safety monitoring, data entry and timely EDC query resolution.