One research network. Multiple ways to use it.
From custom Python analyses to clinical trial recruitment, Tamarin connects research computation with source-connected clinical data and the organizations that control it.
BYOC Research & Model Validation
Bring your own code to the data.
Researchers can run Python-based analyses against approved clinical data without requiring the participating healthcare organization to deliver the underlying patient-level dataset.
Use Tamarin to:
Run custom retrospective analyses
Generate real-world evidence
Test research hypotheses
Validate proprietary algorithms
Validate AI and machine-learning models
Analyze cohorts across participating organizations
Your model stays yours.
Your proprietary model stays yours. Tamarin is designed to keep analytical logic confidential from participating healthcare organizations and Tamarin while providing cryptographic verification that approved code executed in the intended environment.
Trial Feasibility & Site Discovery
Find out where the patients are before opening the sites.
Turn clinical trial inclusion and exclusion criteria into executable queries across participating healthcare organizations.
Three simple steps:
1. Submit a protocol
Tamarin translates the relevant eligibility logic into a computable study.
2. Evaluate participating populations
Approved queries determine approximate eligible populations within participating organizations.
3. Identify promising sites
Sponsors & CROs focus qualification efforts on organizations where relevant patient populations actually exist.
Use cases:
Protocol feasibility
Cohort sizing
Geographic feasibility
Site identification
Site prioritization
Recruitment planning
Clinical Trial Enablement
Move from feasibility to recruitment using the same source-connected infrastructure.
Tamarin keeps healthcare organizations connected after feasibility, supporting patient identification, site-controlled recruitment, and study-specific analysis without requiring a new data integration at every stage.
Tamarin can support:
Patient identification
Run approved eligibility logic against source-connected clinical data.
Recruitment workflows
Allow participating healthcare organizations to act on potentially eligible patient populations under appropriate study and organizational processes.
Ongoing eligibility
Where configured, eligibility logic can be rerun as patient populations change.
Study-specific analysis
Use the same research infrastructure for approved analyses throughout the study lifecycle.
Tamarin complements the sponsor or CRO’s existing clinical-trial infrastructure. It does not replace investigators, IRBs, EDCs, CTMSs, or other systems and processes required to conduct a clinical trial.
Need something more custom?
Tamarin provides study-specific support to researchers and healthcare organizations, including query development, data mapping, study design support, feasibility work, and onboarding of new data sources.