Assess fit, staffing
and operational burden earlier
Built on the Clinials protocol intelligence platform, the profile translates protocol text into a practical view of what a study requires from your site. Investigators understand what matters before the team is committed, not after.
Every output traces back to the protocol, so your team can verify each requirement at its source.
Site selection carries real risk. Most of it is visible in the protocol
Misalignment between what a study needs and what a site can deliver is preventable when the demand is clear at feasibility, not after activation.
37%
Of sites under enrol against their target
11%
Of sites in a typical trial fail to enrol a single patient
One structured document. Every question your feasibility review needs answered
DEMAND, DECODED
Who the study needs
Eligibility thresholds, key exclusions and prior treatment requirements.
Feasibility, in a single review
The questions your team must answer, structured so one review settles them.
What it asks of your site
Procedures, equipment, sample handling and specialist referrals.
Pharmacy and central services
Storage, preparation, IRT, central laboratory and sponsor approvals.
Participant and visit load
Visit schedule, fasting, home assessments and time in study.
See the commitment clearly
Before resources, staffing and patient burden become a guess.
Generate a Site Requirements Profile from your protocol
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