Healthcare

The suites

Each suite is a standalone capability. Adopt one, or run them together as a single operating layer.

1. Suite 01

   Identity & Credentialing

   Patient, provider, and credential verification that holds up across every institution.

   Identity is where healthcare interoperability breaks. Patients are re-verified at every door, provider credentials are re-checked at every network, and every siloed identity database becomes a breach target. This suite provides verifiable, portable identity for patients, providers, and devices — proven without centralizing sensitive data.

   What’s included

   • Verifiable digital identity for patients and providers that holds up across institutions and jurisdictions, designed for portability rather than lock-in.
   • Provider credential and licensure verification — credentials proven current and authentic without repeated manual re-credentialing cycles.
   • Privacy-preserving verification — identity attributes confirmed without exposing or centralizing the underlying personal data.
   • Multi-factor identity binding for individuals, organizations, and connected devices.

   Compliance angle

   Supports HIPAA's minimum-necessary and access-control requirements and identity-proofing expectations, without creating a centralized registry that becomes a breach and audit liability.

   What changes

   Patients and providers are verified once and recognized everywhere, instead of re-proven at every boundary — and the institution stops holding identity data it doesn't need to.

2. Suite 02

   Compliant Data Exchange

   HIPAA-compliant pipelines that carry their controls with the data.

   Clinical, claims, and consent data must move between providers, payers, and platforms — but every exchange is a HIPAA exposure and every consent question is a liability. This suite provides data-exchange pipelines with compliance and consent controls built into the flow rather than bolted on afterward.

   What’s included

   • HIPAA-compliant pipelines for clinical, claims, and consent data, with BAA- and DPA-aligned controls baked in.
   • On-chain enforced, role-based access control — data access rules enforced and recorded at the protocol level, not just by policy.
   • Patient consent tracking — consent capture, scope, and revocation recorded as tamper-evident, timestamped events that travel with the data.
   • Selective disclosure and jurisdiction-configurable data-residency controls so parties collaborate on outcomes without over-sharing inputs.

   Compliance angle

   HIPAA Privacy and Security Rules, BAA obligations, 42 CFR Part 2 sensitive-data handling, and state consent and data-residency requirements are enforced by the exchange itself — every access and disclosure is provable.

   What changes

   Sharing data stops being a multi-week legal and technical project, because the controls and the consent record move with the data.

3. Suite 03

   Records Integrity & Provenance

   Tamper-evident records that turn audit prep into a query.

   Health records must remain trustworthy and retrievable for decades, through system migrations, vendor changes, and litigation — and an institution must be able to prove who accessed what, when, and under what authority. This suite makes record integrity and access provenance cryptographically verifiable and preserves it for the life of the retention mandate.

   What’s included

   • Medical record integrity — tamper-evident proof that a record is authentic and unaltered, detectable to the smallest change.
   • Access and consent provenance — an immutable, timestamped record of every access, exchange, and consent decision.
   • Long-horizon archival designed for multi-decade retention mandates, independently verifiable without depending on any single vendor or system.
   • Regulatory and legal export — proof packages formatted for audit, discovery, and regulatory submission, with independent verification instructions.

   Compliance angle

   HIPAA audit-control and integrity requirements, state multi-decade retention mandates, and breach-investigation and e-discovery obligations are met with evidence-grade records that survive system change and stand up under scrutiny.

   What changes

   Audit prep, breach investigations, and records requests become a query against a verifiable record instead of an archaeology project across dead systems.

4. Suite 04

   Supply Chain & Traceability

   Verifiable chain of custody for drugs, devices, and biologics.

   Counterfeit drugs, recalled devices, and broken cold chains carry patient-safety, regulatory, and financial consequences. This suite provides immutable, verifiable provenance from origin to point of care, with sensor integration for conditions that must be proven, not assumed.

   What’s included

   • Drug and device chain-of-custody tracking — immutable provenance from manufacture through dispensing or implantation.
   • Anti-counterfeit verification at any point in the chain.
   • Sensor and IoT integration for cold-chain and handling conditions, recorded as tamper-evident events.
   • Multi-party audit trail across manufacturers, distributors, pharmacies, and providers without forcing data sharing between competitors.

   Compliance angle

   Supports DSCSA pharmaceutical traceability, UDI device-identification requirements, and recall and adverse-event documentation with a verifiable, regulator-exportable record.

   What changes

   Recalls, counterfeit detection, and cold-chain disputes resolve against a provable record instead of a paper trail across many parties.

5. Suite 05

   AI Operations

   Put AI on prior auth, eligibility, and chart review — with every decision auditable.

   Prior authorization, eligibility checks, coding, and chart review consume enormous clinical and administrative time and are a constant source of payer–provider friction. This suite applies AI to that work, with every AI step constrained, logged, and auditable — so automation reduces burden without introducing unexplained-decision risk.

   What’s included

   • AI-assisted prior authorization, eligibility, coding, and chart review that accelerates throughput while producing an auditable record of every decision.
   • Governed AI steps embedded in workflows, with constrained inputs/outputs, approval gates, and full decision logging.
   • Data-provenance controls so every AI-influenced clinical or administrative outcome has a provable record of inputs, sources, and approvals.
   • Human-in-the-loop gating and reversibility for high-stakes determinations.

   Compliance angle

   Every AI-influenced determination carries a provable record of inputs, outputs, and approvals — aligning with HIPAA accountability and emerging clinical-AI governance and transparency expectations rather than creating a new black box.

   What changes

   Prior-auth and review cycles compress, payer–provider disputes shrink, and AI enters clinical and administrative workflows as an auditable participant rather than an unaccountable one.

6. Professional Services & Lifecycle

   Built around your organization — not the other way around.

   Futures Foundry is founder-platform-native: we build the underlying infrastructure we deploy, so implementations are designed around a health organization's actual environment and regulatory posture rather than forcing the environment to fit a generic product. Every engagement is delivered under a predictable software-as-a-service commercial model.

   What’s included

   • Implementation, compliance design, and architecture tailored to the organization's regulatory environment.
   • Integration with existing EHR, claims, identity, and clinical systems.
   • Custom development and configuration of suites, workflows, and compliance rules.
   • Ongoing maintenance, SLA-backed support, and continuous customization as regulations and operations evolve.