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VT.HCVertical accelerator

Healthcare + life sciences — regulator-aligned by default.

GDPR Article 9 (special-category data) baseline with HIPAA-equivalent controls for cross-Atlantic programmes. NHS DSP Toolkit Standards Met submission, FDA 21 CFR Part 11 audit trail, EU MDR 2017/745 compatibility for medical-device adjacent flows. Customer-cloud (DM.02) for most engagements; DM.04 confidential compute for multi-party clinical research.

VT.HC.FTWhy FlyttGo fits this vertical

Health-data deployments fail more often on data-residency and regulator hand-off than on technology. FlyttGo ships per-region data residency at the audit-envelope level, GDPR Article 28 DPA pre-signed with Article 9 addendum, and a regulator-friendly export pack — so the integrator can focus on clinical workflow, not procurement plumbing.

VT.HC.RGRegulatory framework alignment

6 frameworks pre-mapped to the platform.

  • VT.HC.RG.01

    GDPR Article 9 + Article 28

    European Union

    Special-category personal-data processing terms; pre-signed DPA with Article 9 addendum and EU SCCs (2021/914) for any restricted transfer.

  • VT.HC.RG.02

    HIPAA + HITECH

    United States

    Business Associate Agreement (BAA) available; HIPAA Security Rule baseline mapped through audit envelope + Identra access controls.

  • VT.HC.RG.03

    NHS DSP Toolkit

    United Kingdom · NHS

    Standards Met submission for the Civitas + EduPro surfaces deployed into NHS-adjacent programmes.

  • VT.HC.RG.04

    FDA 21 CFR Part 11

    United States · FDA

    Electronic records + electronic signatures. Append-only audit_log + Identra qualified signatures land Part 11 compatibility for clinical trial workflow.

  • VT.HC.RG.05

    EU MDR 2017/745

    European Union

    Medical Device Regulation interoperability for device-adjacent flows. FlyttGo platform itself is not a medical device; integrators using it for software-as-medical-device need a separate notified-body assessment.

  • VT.HC.RG.06

    ISO 27799 (health informatics)

    International

    Information security management for health informatics. Aligned via the platform-level ISO 27001 ISMS.

VT.HC.MDRecommended module fit
VT.HC.RKSector risk register

4 risks named, with mitigation.

  • VT.HC.RK.01

    Cross-border patient data

    EU patients + US-resident infrastructure is a non-starter under GDPR. FlyttGo enforces region-pinned data residency at the audit envelope; cross-border transfers gated by DPA + SCCs.

  • VT.HC.RK.02

    Clinical research multi-party

    Multi-hospital data unions need to compute without any party seeing the others. DM.04 confidential compute + optional homomorphic-encryption analytics enable this without changing the clinical workflow.

  • VT.HC.RK.03

    Regulator hand-off

    Health regulator audit windows compress timelines. FlyttGo audit envelope exports a regulator-friendly archive (signed manifest + chain-of-custody) on demand; integrators add the clinical-evidence layer.

  • VT.HC.RK.04

    Software-as-medical-device boundary

    FlyttGo is not a medical device. Integrators building SaMD on top need a separate notified-body assessment; FlyttGo provides the audit envelope and identity stack the SaMD assembly needs.

VT.HC.PRProcurement routes
  • NHS Shared Business Services framework
  • EU Health Data Space (EHDS) compatible procurement
  • CCS G-Cloud 14 Cloud Software lot
  • Hospital Trust direct engagement with NHS DSP Toolkit Standards Met evidence
VT.HC.CSReference programmes in this vertical
VT.HC.NX · vertical-aware engagement

Open a programme on this vertical's terms.

Consultation routed to the desk handling healthcare + life sciences programmes. DM.02 substrate, L.05 tier and the regulatory framework matrix above presented at intake — scoping starts at SE.D2, not at framework discovery.

Open consultation · CB.00Generate a CAIQ for this vertical · AS.00All verticals