Our Feasibility Services provide sponsors with a clear, evidence-based assessment of whether a study can be delivered on time, on budget, and to protocol. We focus on early-phase and complex clinical trials where operational accuracy and realistic planning are critical. We translate protocol concepts into practical execution plans by evaluating scientific, operational, and regulatory factors before study start.

‍Protocol review & complexity assessment
Identification of critical procedures, dosing schedules, PK intensity, and operational risk drivers.
Population & recruitment analysis
Availability of eligible subjects, screen-failure risk, recruitment timelines, and retention considerations.
Site & capacity assessment
Bed capacity, staffing, equipment, pharmacy, laboratory, and scheduling feasibility.
Operational timelines
Realistic projections for start-up, screening, dosing, follow-up, and database readiness.
Regulatory & ethics readiness
Anticipated submission timelines, country-specific requirements, and approval risks.
Budget & resource alignment
Validation of cost assumptions against actual workload and infrastructure needs.
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Early feasibility prevents under-scoping, avoids costly amendments, and supports confident internal decision-making. Our approach is conservative, transparent, and grounded in real operational experience—ensuring your study design is not only scientifically sound, but executable in practice.