For pharma & research
Pre-consented cohorts from our biobank. You define the criteria, we find the patients. Pay only when the cohort meets your protocol.
Traditional CRO
acta.bio
What you get
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.
Therapeutic Areas
Data Types Included
Avg Record Depth
Median 2,847 data points per participant
How it works
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. As specific as your protocol demands.
Our matching engine queries our pre-consented pool. Eligible participants are verified and enrolled automatically.
Full preview in our secure data environment. Inspect demographics, distributions, and data completeness before committing.
Only when the cohort meets your protocol requirements. No obligation until you're satisfied with the data quality.
The biobank
Individuals
Countries
Consent retention
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.
Tell us what you need. We'll show you who's available.
GDPR Art. 7 · EU Clinical Trials Regulation · ISO 27001 · Your data never sold without consent