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.

Yes.

Feasibility responses are typically delivered within days and include:

• Recruitment projections
• Inclusion/exclusion considerations
• Operational and logistical requirements
• Site capabilities
• Timeline expectations

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

Pricing is based on:

• Study procedures and complexity
• Sample or visit volume
• Processing and logistics requirements
• Recruitment expectations
• Study duration

We provide transparent quotes and support iterative revisions.