We recruit:

• Healthy volunteers
• acutely or chronically ill adults
• Pregnant or postpartum individuals (if applicable)
• Diverse demographic and socioeconomic populations
• Disease-specific cohorts
• Rare and hard-to-recruit indications

Recruitment is tailored to each protocol.

We provide a full suite of regulatory and site documentation, including:

• IRB approvals
• ICF versions
• Investigator CVs, licenses, training certificates
• Delegation logs
• SOP summaries
• Regulatory binder contents
• Laboratory certifications (as applicable)
• CLIA-related documentation
• Site qualification materials

We support:

• Phase II–IV clinical trials
• IVD and diagnostic performance studies
• Device usability and human factors research
• Prospective biospecimen collection studies
• Observational and registry-based research
• Retrospective biospecimen retrieval
• Longitudinal and multi-timepoint sampling

Our integrated CRO + clinical site model allows for rapid, consistent, and high-quality study execution.