For the complete documentation index, see llms.txt. This page is also available as Markdown.
Medical study and clinical document
Review synchronized medical imaging and clinical documentation as one governed case.
Use a medical Data Group when imaging, synchronized projections, sequences, and supporting clinical documentation must stay together. The active medical editor creates geometry and clinical values; document panels preserve report, page, and contextual evidence.
See the medical workflow
Synchronized axial, coronal, sagittal, and 3D DICOM views
One study remains available across complementary views while the active editor controls annotation.
Design the case
Include only the sources allowed by the project’s privacy and access policy. Define:
the study and series identity;
which DICOM views or sequences belong together;
which report or clinical document provides supporting context;
whether the document is evidence, ground truth, or a source for separate labels;
the clinical ontology and required properties;
the specialist review and escalation path;
redaction or de-identification requirements.
Work through the group
1
1. Confirm case identity
Verify the study, series, document, and project-safe identifiers before viewing or annotating protected data.
2
2. Inspect synchronized imaging
Navigate axial, coronal, sagittal, 3D, or sequence views to understand the finding in full context.
3
3. Consult the clinical document
Open the relevant report page or text window. Keep a clear distinction between a visible finding and an interpretation stated in the document.
4
4. Create the clinical annotation
Activate the medical view, choose the ontology class, create geometry, and complete visible-morphology properties.
5
5. Add governed context
Use Item Properties or relations for study-level and cross-source information. Do not copy free text into structured values when the ontology requires a controlled choice.
6
6. Specialist review
Inspect cross-view extent, sequence continuity, document consistency, uncertainty, validation, and provenance before routing the group to approval.
Clinical quality boundary
Supporting documentation can inform review, but the project must define whether a label represents image evidence, a clinician’s interpretation, or a combined adjudicated result.
Preserve study and series identity, source document and page, geometry, clinical properties, relations, reviewer provenance, ontology version, and group membership in downstream dataset versions and releases.
