For sponsors & CROs
Site capabilities
Infrastructure, staffing, and quality systems in one place.
Infrastructure and equipment
Our facility supports outpatient protocols requiring standard assessments, sample processing, and controlled storage.
- Private assessment and consent rooms
- Temperature-monitored refrigeration and freezer capacity
- Centrifuge and on-site sample processing
- ECG capability and calibrated vital signs equipment
- Access-controlled document storage
- Dedicated monitor workspace with connectivity
Staff and credentials
Principal Investigators, sub-investigators, certified coordinators, and a dedicated regulatory manager. Training records, CVs, and delegation logs are maintained per protocol and available for review.
Recruitment and retention
Recruitment combines a consented site database with community outreach and bilingual materials. Retention is supported by flexible scheduling, appointment reminders, and consistent coordinator assignment across a participant's visits.
Frequently asked questions
Answers to questions we hear most often.
What is your recruitment database size?
Current database figures, along with historical enrollment against target by therapeutic area, are shared during feasibility review.
What is your typical enrollment timeline?
Timelines depend on protocol criteria and competing studies. We provide realistic, protocol-specific projections rather than generic estimates during feasibility.
How do you manage protocol deviations?
Deviations are documented, reported to the IRB and sponsor per requirements, and reviewed internally with corrective action where appropriate.
Do you support electronic data capture systems?
Yes. Our coordinators work across common EDC and ePRO platforms and complete system-specific training before enrollment begins.
Can you support studies requiring longer visits?
Yes, within our facility's capacity. Extended-visit requirements are assessed during feasibility.
Want the full capabilities packet?
We can share equipment lists, CVs, and site experience summaries under confidentiality.
Request the packetInformation on this website is provided for general educational purposes about clinical research and is not medical advice. Participation in any study is voluntary.