A diagnostic lab builds patient matching logic. A pharma company builds it again for their trials. A cell therapy manufacturer builds it again for chain-of-identity. A CRO builds it again for regulatory submissions.
Same problem, solved independently, four times.
Every organization in precision medicine rebuilds the same execution infrastructure: onboarding, lineage tracking, validation, compliance.
The patient matching logic that a diagnostic lab builds to link specimens to patient records is functionally identical to the patient matching logic that a CRO builds to link trial subjects to enrollment records. Both resolve names, dates of birth, MRNs, and specimen IDs against a canonical identity. Both handle edge cases: name changes, transfers between facilities, multiple specimen types. Both need to be auditable. Neither organization can reuse the other's implementation, because there's no shared layer to build on.