Enter your eligibility criteria. TrialBridge returns a defensible feasibility estimate: patients we can observe today, plus the addressable market with a confidence interval — mapped to region and candidate sites.
The real bottleneck isn't discovery — it's matching. We turn two-sided free text (your criteria and Brazilian clinical records) into one computable OMOP layer, then count.
Biomarkers, staging, performance status and prior lines of therapy, extracted from Portuguese clinical notes by NLP. It's the granularity administrative data can't see.
The overlap between our clinical base and DataSUS is a Rosetta Stone: we learn the mapping once, then report site-level patients we can observe directly and a calibrated national estimate.
Loosen a single eligibility criterion and watch the eligible pool expand across responding sites. Only possible with clinical depth — administrative data can't see the criterion that actually gates enrollment.
Share your indication and key criteria. We'll come back with a first-pass Brazil feasibility read — observed and estimated N, with candidate regions.
In the live version, your study lands in the TrialBridge queue and you get a first-pass Brazil feasibility read by email.