Sovereign healthcare data infrastructure for AI-ready research
MedSyntra enables governed, auditable access to clinical imaging and healthcare data—without compromising privacy, control, or data sovereignty.
What we do
A platform + data access model
MedSyntra combines sovereign infrastructure with governed data access, so institutions retain control while research and innovation can move faster.
Platform deployments
Deploy MedSyntra as sovereign data infrastructure for institutions or national frameworks—supporting residency, control, and auditability.
Governed data access
Request research-ready cohorts curated from indexed archives—delivered through controlled packages or API access.
De-identification by design
Privacy-first processing designed for research workflows, including metadata and pixel-level de-identification.
Smart indexing & cohorts
Structure and enrich imaging archives to enable fast cohort building and reproducible research selection criteria.
Secure delivery & audit trails
Controlled access, traceability, and clear governance—supporting compliance requirements and responsible use.
Contributor monetization
Enable clinics and hospitals to participate in monetization under agreed terms—without losing ownership or control.
How MedSyntra works
1) Ingest
Connect imaging and clinical sources (e.g., DICOM and HL7) and ingest into a governed research pipeline.
2) De-identify
Apply privacy controls designed for research use, including metadata and pixel-level de-identification.
3) Enrich & index
Extract structured signals and index studies to support fast search, filtering, and cohort generation.
4) Build cohorts
Create research-ready cohorts using defined inclusion/exclusion criteria and governance approvals.
5) Deliver securely
Deliver via controlled packages or API-based access with audit trails and contractual governance.
Platform
Sovereign deployments for institutions and national frameworks
Deploy once. Enable many.
A single platform can support multiple research programs, AI development efforts, and governed cohort requests—while keeping control in the hands of local institutions.Deployment options
Deploy in-country or within required regions to support sovereignty and residency requirements.
Separation from clinical operations
Designed for research and innovation workflows—separate from diagnostic clinical systems.
Governed access models
Institutional approval, auditability, and clear access controls aligned with compliant research workflows.
For contributors
Monetize responsibly while retaining ownership and control
You stay in control
Access is governed and auditable—aligned to institutional approval and agreed policies.
Privacy-first processing
De-identification designed for research use, with strict handling of metadata and pixel data.
Revenue participation
Contributors participate in monetization based on agreed commercial terms and measurable usage.
Low operational overhead
We manage ingestion, processing, indexing, cohort creation, and secure delivery.
FAQs
Frequently asked questions
Clear answers about platform deployments, data access, and contributor participation.
Is MedSyntra a platform or a data provider?
Both. MedSyntra can be deployed as sovereign infrastructure, and it can also provide governed data access through cohort requests and curated datasets.
Who owns the data?
Contributing institutions retain ownership. Access is governed through agreed policies, approvals, and auditability designed for responsible research use.
Do you centralize data outside the country?
MedSyntra supports sovereign deployment options where data residency and national control are required. Deployment models are defined per project and jurisdiction.
How do we request data access?
Start with the Data Access page to outline your cohort needs. We align on criteria, governance approvals, delivery method, and timeline before any access is granted.
How can clinics monetize their data?
Contributors participate in monetization under agreed commercial terms. MedSyntra handles processing, indexing, and delivery so contributors can participate with low operational burden.
Build trust.
Enable research.
Start with a platform deployment, request a cohort, or become a data contributor. We’ll help you choose the right model and move forward safely.