Pre-consented cohorts from our biobank. You define the criteria, we find the patients. Pay only when the cohort meets your protocol.
Every participant has given explicit, granular consent under GDPR Article 7 and the EU Clinical Trials Regulation. Records are verified against primary sources, with full chain-of-custody documentation. Genomic, clinical, and wearable data layers are linked and de-identified to your specification.
Median 2,847 data points / participant
No retainers, no monthly fees, no platform subscriptions. You pay only when a delivered cohort meets your protocol requirements.
Demographics, conditions, biomarkers, inclusion/exclusion criteria.
Matching engine queries our pre-consented pool. Participants enrolled automatically.
Full preview in our secure data environment. Inspect before committing.
Only when the cohort meets your protocol requirements. No obligation until you're satisfied.
An early biobank built from explicit, granular consent under GDPR Article 9. Help define what gets built first — your protocol shapes the next data layer we prioritise.
Data never leaves our secure environment. Your researchers get full analytical tooling in a compliant, audited workspace. No data extraction, no USB drives, no risk.
Full audit trails on every query. Differential privacy available. Data linkage without re-identification.
Start your own small pharma revolution. Backed by participants who care.
GDPR Art. 9 · EU Clinical Trials Regulation · Patient-consented cohorts
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