Access
Role and need-to-know access can be defined for the pilot environment.
Security
Research controls should be explicit before any data is exchanged.
Introute Medical supports controlled research environments. The precise technical and contractual boundary is defined for each pilot based on the sensitivity of the approved inputs and the selected inference route.
Data boundary
Collect only what the pilot requires.
Data minimisation begins during scope definition. Approved datasets, prohibited content, transfer method and permitted use are documented before work starts.
Inference boundary
Know where each computation happens.
The model and evidence route is configured with the required privacy boundary. External services are included only when approved and appropriate to the pilot.
Traceability
Relevant processing steps and output provenance are retained for research review.
Retention
Retention and deletion are agreed, not assumed.
Input, intermediate and output retention periods are part of the pilot terms. Data processing, access rules and project closure procedures are defined in advance for the needs of each research programme.
Controlled operations
Trust is built through clearly defined controls.
Security and operating requirements are translated into a concrete environment configuration, access model and documented procedures for each Research Pilot.
Introute Medical · Intelligent routing for biomedical discovery.
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