Governed data access
Request research-ready cohorts and datasets under governance-first access models. MedSyntra supports compliant, auditable delivery—so research teams can move faster without compromising trust.
What you can request
Cohorts built for AI training, validation, and research
Define your criteria, align on governance, and receive secure access through approved delivery models.
Cohort definition
Specify modality, anatomy, timeframe, demographics (where allowed), and inclusion/exclusion rules.
Research-ready packaging
Structured exports and documentation that support reproducibility and regulated workflows.
Secure delivery
Controlled delivery via secure packages or API-based access with auditability.
Optional annotation
Where needed, radiologist-led annotation can be arranged for selected cohorts.
Longitudinal support
Support for follow-up studies and longitudinal research selection (where available and governed).
Compliance-first approach
Access models designed around governance, approvals, and traceable usage—aligned to responsible research.
How data access works
1) Describe your use case
Tell us what you’re building or validating and what cohort criteria you need.
2) Define criteria and scope
We align on inclusion/exclusion criteria, formats, delivery model, and timeline.
3) Governance & approvals
Access is governed through approvals and agreed policies before any delivery occurs.
4) Build and validate the cohort
We generate the cohort from indexed archives and prepare the access package or API permissioning.
5) Deliver securely
You receive controlled access with traceability and clear usage terms.
Delivery models
Secure access that fits your workflow
Built for governed research access
We’re not a “data dump.” MedSyntra is designed to enable responsible access under governance—so institutions can participate and researchers can trust what they receive.Secure dataset packages
Cohorts delivered as controlled exports with clear documentation and agreed usage terms.
API-based access
Access via governed APIs where appropriate—built for traceability and controlled consumption.
Evidence-ready processes
Support workflows that require reproducibility, auditability, and strong governance controls.
FAQs
Data access FAQs
Practical answers for AI teams, researchers, and regulated workflows.
What kinds of cohorts can you provide?
Cohorts are defined by your criteria (modality, anatomy, timeframe, and other governed fields). Availability depends on contributor sources and approval models.
Can you provide annotations?
Yes, for selected projects we can arrange radiologist-led annotation or structured labeling—subject to scope, governance, and availability.
How is access governed?
Access is governed through agreed policies, approvals, contractual terms, and auditability designed for responsible research use.
Do you support data residency requirements?
Yes. When residency or sovereignty is required, we can align delivery and deployment models accordingly.
How do we get started?
Use the “Request a cohort” contact path with a brief description of your use case and criteria. We’ll respond with next steps and the information needed to proceed.
Move faster—without compromising trust
Tell us what you need: training data, validation cohorts, or regulated evidence packages. We’ll help you define a governed path to access.