What the programme covers
The phrase US-sourced can refer to care location, source organization, patient population or permitted processing and delivery. A sound feasibility process resolves those meanings and verifies the operational path rather than assuming that a country label proves availability.
What a useful specification includes
A defensible request defines the clinical task, source evidence and acceptance criteria before patient-level data moves. The exact fields and thresholds depend on the intended model claim.
- US care setting, population and site requirements
- Modality, anatomy, pathology and acquisition details
- Case definitions and reference-standard evidence
- Required reports, pathology, outcomes or annotations
- Intended use, recipient, processing and delivery constraints
- Target volume, timeline and validation design
Quality and validation controls
Each feasibility statement is assigned a status: verified inventory, inventory under verification, sourcing scope or buyer-specific feasibility. This prevents early source indications from being repeated as deliverable cohort claims.
- Meaning of US-sourced documented
- Candidate site and inventory status separated
- Case-count logic and counting unit recorded
- Ground truth and permission path checked
- Unresolved assumptions and timeline dependencies listed
Availability, rights and delivery
If feasibility is positive, programme-specific authorization, privacy controls, technical acceptance and licence terms must still be completed before an approved release.
Public pages describe a sourcing and engineering capability, not guaranteed ready inventory. Each release remains subject to verified programme inventory, programme-specific authorization, privacy review, technical acceptance and buyer licence terms.
Questions, answered directly.
Does MedCorpora already hold every US imaging cohort?+
No. US requirements are assessed and pursued through buyer-specific feasibility; availability is not assumed.
Can a US request include longitudinal outcomes?+
It can be requested, but source coverage, linkage, permissions and follow-up must be verified.
What is the first information a buyer should provide?+
Modality, pathology, cohort definitions, ground truth, geography, intended use, required components, approximate size and timeline.
When does patient-level data move?+
Only after the appropriate programme authorization and technical controls are established.