Documents Initial use case
- secure upload;
- a limited set of formats;
- recognition with verification;
- links to the source and version.
Integrations and API
For each data flow, we define field meanings, sources, units, access rights and error handling in advance.
The public API is not yet open. A test environment is available as part of a pilot.
Who needs the data, and for which process.
Schema, units, identifiers and versions.
Roles, consents, tenant and processing period.
Errors, retries, audit and stop criteria.
Integration options
Data scope, security and operational readiness are confirmed separately for each channel.
Data contract
A minimum contract must make clear what was transmitted, its source, when it was recorded, its units and the basis for processing it.
Association with a person or episode without silently mixing records.
Organisation, document, device, author and precise event time.
A value is interpreted only together with its term, unit and applicable reference range.
A correction creates a new version and retains its link to the previous one.
Data transfer is limited by the use case, role, consent and duration.
An unknown field, duplicate or conflict does not automatically become a medical fact.
Integration stages
Each stage begins only after the previous one has been checked.
Purpose, users, owners and scope.
Sources, fields, terminology and quality.
Access, transfer, storage and incident response.
A limited data flow, test data and success criteria.
Monitoring, versions, support and a decision on scaling.
Responsibilities
An integration is not complete until the parties know who is responsible for the source, field mapping, access and failure response.
Medical data must retain its meaning and provenance. The recipient of the result and its review status must also be defined in advance.
Source quality, lawful transfer and notification of changes.
Ingestion, contract validation, data provenance and controlled processing.
Clinical rules, staff permissions and medical review.
Incidents, schema changes, stop criteria and scaling.
Technical readiness
Materials are provided after the use case is defined. Real medical data is not shared at the initial stage.
A source, a contract, security and a measurable result.