Sponsors & CROs

Site feasibility

Before you finalize a site list, see which participating sites have patients likely to qualify for your protocol, how many, and which other studies are recruiting them.

Site feasibility for a phase 3 KRAS G12C NSCLC trial: candidate sites ranked by estimated 12-month enrollment, with the Trova assistant explaining one site’s estimate

The product

Pick sites that can
actually enroll.

Four things this use case does to replace questionnaire guesswork with evidence when you select sites for a new trial.

Your protocol, tested across sites

Run draft eligibility criteria against participating sites and see which criteria shrink the eligible pool most — before the protocol is locked

Protocol criteria showing how much of the eligible pool each one removes, and how relaxing the PD-L1 threshold lifts potential enrollment from 56 to 130 patients across six sites
  • Eligible patients by site

    De-identified, aggregated counts of likely-eligible patients at each participating site, from their current records.

  • Competing studies in view

    See where your target population is already being recruited by other trials, so you avoid sites that will struggle to enroll.

  • Faster feasibility, fewer surveys

    Shortlist sites from data instead of chasing feasibility questionnaires, then confirm with the investigators you want.

In practice

CROs that select sites on evidence

We used to choose sites from feasibility questionnaires and hope. Now we start from real eligible-patient counts, and the sites we activate actually enroll.
Sophie K.
Feasibility Lead

2×

faster site selection

Find sites that will enroll.
Before you activate them.

Bring us your next protocol and we’ll walk you through site feasibility for it. Centrova is working with a small group of early sponsor and CRO partners.

Talk to our team

Book a demo

See how Centrova helps your research team find eligible patients and fill trials sooner.

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