A programme begins at the hospital source
The platform establishes what a hospital archive contains, which authority applies and how studies, reports and clinical evidence can be resolved into governed programme inventory. Detection, segmentation, quantitative and foundation-model workloads are then materialized from that controlled source layer.
Each programme publishes its composition, missingness, privacy controls, clinical review standard and release history. Availability is established through the programme control plane rather than inferred from raw file counts.
What can be specified
Each programme can be narrowed by anatomy, pathology, scanner vendor, field strength, sequence or reconstruction, contrast status, population distribution, clinical evidence and permitted commercial use.
- Brain MRI with T1, T2, FLAIR, DWI/ADC and selected perfusion
- Liver MRI/MRE with disease-defined cohorts and matching sequences
- Non-contrast CT for cardiovascular, lung, bone or body-composition tasks
- Additional modalities and linked clinical records where hospital programme controls are established
No silent substitution
A missing sequence, report or demographic field changes whether a cohort is fit for purpose. Dataset cards therefore record what exists, what was excluded and what remains unknown. Derived files never replace source acquisition records without an explicit release definition.
Questions, answered directly.
Are all programmes immediately available?+
Programme composition and access are confirmed under individual governance, diligence and licensing processes rather than through public downloads.
Can a programme be exclusive?+
Exclusivity can be discussed, but it changes hospital permissions, commercial terms, duration and price. Non-exclusive licensing is the default structure under consideration.
Do you provide a pilot?+
The intended process is a small, privacy-cleared sample assessed against written acceptance criteria before a final cohort is prepared.