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Shivya Technologies

Use case · Healthcare / Life Sciences

Clinical & Regulatory Evidence Copilot

Nothing enters a generated document without a verifiable source. The model drafts. A qualified human signs off.

8–15 min
Patient narrative authoring time, review + edit (target, from 45–90 min)
3–5 weeks
Document first-draft cycle time (target, from 8–14 weeks)
<0.2 / document
Numeric errors reaching medical review (target, from ~2.4 / document)
<1 / document
Cross-section inconsistencies at QC (target, from ~6 / document)
12–18 hours
Literature screening time per cycle (target, from 60–80 hours)

The problem

A wrong number here isn't a bug. It's a data-integrity event.

  • Documents take weeks

    Producing a regulatory study report pulls in medical writers, biostatisticians, and physicians for weeks — much of it spent assembling and cross-referencing, not writing.

  • Patient narratives are the worst of it

    A single study can need hundreds of similar narratives, each reconciling demographics, history, medications, and a chronological event account from several source systems.

  • Source data is scattered

    Structured clinical datasets, scanned forms, lab reports, and safety database extracts — no single queryable surface ties them together.

  • Inconsistency triggers rework

    A figure in the summary that doesn't match the results table is a recurring finding that sends a whole document back through review.

The high-level solution

A five-layer, grounded generation architecture.

Nothing enters a generated document without a verifiable source reference. The output is a draft for a qualified human — never an auto-approved regulatory document. That framing is both scientifically and legally correct.

  • Evidence & retrieval

    Every source — structured datasets, scanned documents, literature — is normalised into an evidence base where every atomic fact carries a provenance record back to its source.

  • Structured generation

    Documents are generated section by section against a template that defines required content and constraints. The model writes prose; every number is injected from a deterministic calculation, never invented.

  • Verification & authorship

    An automated pass checks every number against its source and every section against every other before a human ever sees the draft. The writer edits and signs off — the system never auto-approves.

Architecture

From scattered sources to a signed-off document.

  • Ingestion

    Source systems (clinical, safety, scans, literature) → normalization & provenance tagging → unified evidence base. Every evidence record is immutable — corrections create a new version with a supersession link, never an overwrite.

  • Generation

    Document template → evidence retrieval → deterministic aggregation → grounded generation → automated verification. Pass → writer review. Fail → regenerate with the verification feedback, then escalate with the raw evidence attached after two attempts.

Pipeline

How it got built.

  • Foundation

    Secure storage with immutable retention, a clinical database, and role-based access control.

  • Evidence model

    Provenance-tracked, immutable evidence records — the schema every later stage depends on.

  • Structured ingestion

    Clinical datasets loaded and validated against their declared standard before anything reads from them.

  • Deterministic aggregation

    Every statistic — counts, percentages, incidence rates — computed in code as a named, versioned, unit-tested function. Built before generation, not after.

  • Verification service

    Numeric grounding and cross-section consistency, also built before generation — it defines the contract generation has to satisfy.

  • Templates & generation

    Section-by-section generation contracts, with mandatory citation tokens on every factual claim.

  • Writer workbench

    Citation-linked review, track-changes editing, and a formal sign-off workflow.

  • Literature surveillance

    A scheduled pipeline that screens and summarises new literature for periodic safety reporting.

Outcomes

What moved.

Figures are illustrative engineering targets for this solution pattern, based on comparable production systems — not a guaranteed result for any specific deployment.

  • Patient narrative authoring time

    Before: 45–90 min → Target: 8–15 min (review + edit)

  • Document first-draft cycle time

    Before: 8–14 weeks → Target: 3–5 weeks

  • Numeric errors reaching medical review

    Before: ~2.4 / document → Target: <0.2 / document

  • Cross-section inconsistencies at QC

    Before: ~6 / document → Target: <1 / document

  • Literature screening time per cycle

    Before: 60–80 hours → Target: 12–18 hours

Components

Multimodal document processingMedical entity recognition & de-identificationRelational clinical data storeVector + lexical retrievalGrounded generation with tool useRegulatory-template document assemblyImmutable, tamper-evident retention

This engagement ran AWS-native, matched to the client's existing cloud estate — the same pattern deploys equally well on Azure or GCP.

Where the platform fits

Every pattern here has an action boundary — a block, an approval, a reply. That is exactly where Nikash's gate sits: claims checked deterministically before the action, and real outcomes fed back afterwards.

See the platform →

Have a workflow like this?

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