Special-category data, every record
UK-GDPR handling of special-category data with ICO scrutiny. Consent-aware retrieval is non-negotiable; privacy masking is the default, not the exception.
The patient is waiting. The clinician is three clicks from the report. The hospital runs on half a dozen systems that were never meant to speak to each other. We are the intelligence layer that sits behind EMR, EHR, PACS, LIMS, RIS and HIS — not a ninth system to log into. Built for accreditation cycles (CQC, JCI, NABH), interoperability mandates (FHIR, ONC) and pharma IDMP compliance.
We do not add a ninth system. We connect the eight you already run.
Six structural problems we hear repeatedly from hospitals, clinical networks and pharma — and the honest answer to each.
UK-GDPR handling of special-category data with ICO scrutiny. Consent-aware retrieval is non-negotiable; privacy masking is the default, not the exception.
CQC, JCI, NABH accreditation cycles. The pack has to be assemblable on the day, not produced over six weeks before the inspection.
NHS Digital / NHSX standards, DSPT and DCB0129 / 0160 for clinical safety. MHRA and ICH-GCP for trials; IDMP for pharma. The safety case is the deliverable.
Patient data fragmented across EMR / EHR, PACS, LIMS, RIS, HIS and specialty systems. The clinician spends the consult finding the record.
Handwritten observations, multilingual clinical documentation, historic medico-legal records deteriorating in storage.
Pathology, radiology, cardiology systems with decades of data and no federated retrieval. FHIR and ONC mandates land on top of the existing stack, not instead of it.
Three workstreams that run together. The output is one connected clinical operating layer — not a stack of pilots.
Patient dashboards. Clinician cockpits. Remote patient monitoring apps. Retinopathy and medical-imaging analysis. BIM for hospital design — space, flow and staff efficiency modelled before construction.
Clinical-note summarisation. Priority-of-care triage. Prior-authorisation agents. Multilingual translation at point of care. Research-insight discovery across the clinical corpus.
EMR / EHR (Epic, Cerner, Meditech, TPP SystmOne, EMIS), PACS (GE, Philips, Siemens), LIMS, RIS, HIS, NHS Spine, FHIR / HL7 interfaces.
The Actigen module for hospitals, clinical networks and pharma. Sits behind your clinical systems and makes the document estate searchable, extractable and discoverable.
View the platformA complete healthcare document pipeline. Patient records, radiology and imaging archives, clinical-trial documentation, lab and pathology records, historic medico-legal files. Privacy-by-design and consent-aware retrieval are defaults; FHIR and IDMP exports already wired in.
Six briefs we are running this year — each anchored in a specific clinical or research outcome.
AI and GIS for underserved regions. Outcome data fed back into the clinical record, not stranded in the device.
Patients tracking their own journey; clinicians tracking cohorts. One platform, two audiences.
Space, flow and staff efficiency modelled before construction — not after the cost overruns.
AI on eye scans, X-ray, CT and MRI — early enough to protect vision, with clinician on the gate.
Patients understood in their own language. The translation cited, the consent recorded, the audit retained.
Records from decades back, deteriorating in storage. Scanned, indexed, signed, and migrated — on-site where the records cannot leave.
Three outcomes consistently reported across healthcare engagements. Per-engagement targets agreed in writing during Discover.
30% faster clinical decision support. The clinician sees the record, not the search bar. Retrieval becomes seconds, not clicks.
40–60% lower operational cost on document-heavy administration. Surge capacity on accreditation cycles becomes optional.
80% improvement in research insights through federated search. The corpus stops being where research goes to die.
Numbers that map to how clinical and pharma leaders report up — trust boards, clinical commissioners, regulators.
Actigen 2.0 is the agentic decision-loop framework underneath every engagement. Configurable per industry; consistent in lineage, governance and audit posture. Below: the full platform, with the Healthcare module highlighted.
Libraries, archives, publishers. HWR, IIIF, MARC / EAD / METS, paleography console.
/ A·fBFSI. KYC, claims triage, contract abstraction with audit-pack lineage.
/ A·hHealthcare. Clinical-note summarisation, IDMP, FHIR-mapped knowledge assistants.
/ A·eOil & gas, utilities. CSRD / SEC Climate drafting, asset-document agents, HSE.
/ A·mEngineering knowledge, supplier IP, IATF audit drafting and CAD-aware retrieval.
/ A·uNAAC narratives, ABET evidence packs, credential registries and reviewer copilots.
/ A·rAcademic research operations — TEI, scholarly editions, critical apparatus, IIIF.
/ ePLegislatures, registries, parliaments. Multi-script archives and lawmaking copilots.
"The same loop runs every brief. Only the domain model and the schema mapping change."
View the platformExternally verifiable credentials and the standards every output is engineered to satisfy. The audit pack travels with the system.
External audits aligned to ISO 27001 and 27701. DSPT and NCSC CAF. Special-category data handling with consent-aware retrieval as default.
UK clinical safety standards, accreditation frameworks, pharma compliance — all aligned by default.
Consent-aware retrieval, privacy masking, audit trails by default — the artefacts every clinical commissioner now expects.
“Two hundred thousand medico-legal records back to 1971, deteriorating in storage. SBL scanned, indexed and migrated the collection on-site — the records never left the building. Retrieval moved from hours to minutes. The medical-legal team got their week back.“Director of Medical Records Teaching hospital · medico-legal record digitisation
Send a brief. Receive a measured pilot proposal within the working week.
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