Anurag Jha
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NeuroDiscovery AI · 2026 · B2B · Enterprise AI platform, real world evidence

NeuroAudit

first prototyped as NeuroValidate

An LLM platform that reads millions of clinical notes, answers a study question for every patient, quotes the sentence that proves it, and puts a human reviewer in charge of the final call.

My roleProduct owner from the first line of code. I built the prototype myself.

2.5Mclinical records processedProduction database, all time to Jul 2026
23K+decisions signed by human reviewersProduction database, all time to Jul 2026
462projects, 2,095 AI runsProduction database, all time to Jul 2026
84.9%of records needed no reviewer, lead criterion of a flagship studyStudy brief, Apr 2026
The review screen in front, the projects board and the cohort funnel behind. Real app, demo data, names redacted.

The challenge

Analysts read charts by hand to answer questions like "who stopped this therapy, and why". About 3 hours per 100 patients, not reproducible, not auditable.

What shipped

Four flows on one pipeline: cohort validation, score extraction, anonymisation and trial screening, with cost gates, approvals and model comparison.

What moved

2.5M clinical records processed, 23K+ reviewer decisions, 84.9% resolved with no reviewer time on the lead criterion of a flagship study

The answer to most real world evidence questions is not in a structured field. It sits in a doctor's note, where stopped, held, switched and missed a dose look alike and mean different things.

I built NeuroAudit so a model proposes and a person decides. Every answer carries the exact quote behind it, every run shows its cost before it starts, and nothing leaves the platform without a reviewer's signature.

A

Set up a study

From an empty board to a study with criteria, sources and validated keywords in about ten minutes.

  1. 01

    One workspace for every study

    Each card shows the client, the data sources, the patient count, the team and how far the study has got.

    Projects home. Client, drug and lead names redacted.
  2. 02

    Name the study

    Pick the study type: real world evidence, or a clinical trial cohort.

    Create project, step 1.
  3. 03

    Define the criteria

    Each criterion gets its own data source, scope, providers and keywords. The page always shows which index it will read.

    Criteria and data sources. Partner site names redacted.
  4. 04

    Let an agent check the keywords

    An agent flags keywords that are too broad. Broad keywords do not give wrong answers; they give huge, slow, expensive ones.

  5. 05

    Pass the fetch gate

    Pulling more than 500 patients needs approval, counted with a cheap count only query before any data moves.

    The fetch gate.
B

Run it with cost control

Two prompts per criterion, a model per criterion, and the price on screen before anything runs.

  1. 01

    Home base for the study

    Runs by criterion, model comparisons and the criteria list on one page.

    Project overview.
  2. 02

    Two stage prompts

    One prompt extracts the evidence, a second checks it. Each stage picks its own model, and a model swap has to beat the baseline in a blind comparison.

    Prompts and models. Drug names redacted.
  3. 03

    Scope and mode

    Sample, specific patients or a full run. Fast for small checks, batch at about half the cost for big ones, with personal data removed first.

    Run configuration.
  4. 04

    The cost gate

    Every run shows its estimate. Up to $100 runs on its own; above that, or any full run, needs an approver.

    Cost estimate and limits.
  5. 05

    Approvals

    The approver sees the cost, the scope and why approval was needed, and starts the run with one click.

    The approver's view.
C

Review: the human signs off

The deliverable is the reviewer's decision, not the model's output.

  1. 01

    Evidence, note and verdict side by side

    Green quotes support the answer, red quotes argue against it. The reviewer marks Eligible, Ineligible or Unclear.

    Three pane review. Drug and protocol names redacted.
  2. 02

    A verdict needs a reason

    Every decision carries a note, written to the audit trail.

    Reviewer notes are required.
  3. 03

    Split the work

    Assign groups of patients to reviewers and watch progress live.

    Assignment and progress.
  4. 04

    Built for long review sessions

    Reviewers spend hours in this screen, so every page works in light and dark.

    The same review screen in light and dark.
  5. 05

    Prove a model change

    An LLM judge grades two runs on the same records, blind. This is the evidence for changing a production model.

    Run comparison on a demo study: wins, losses, ties and the judge's reason for each record.
D

Three more flows on the same pipeline

Score extraction, anonymisation and trial screening reuse the same engine.

  1. 01

    Score extraction

    Pull every clinical score (MoCA, MMSE, MIDAS, PHQ-9) from every note, each row with its own justification, then push the table to search.

    Scores review.
  2. 02

    Anonymisation

    Map each source column to a cleaned column, one prompt and one model per column. Clinical meaning survives; names, record numbers and birth dates do not.

  3. 03

    Trial screening

    Every patient against every criterion in one matrix, then a funnel that shows who survives each criterion and why. The funnel is what goes to the sponsor.

  4. 04

    Agents, prompts and data

    An agentic studio to test validation agents, a prompt library so teams reuse what works, and a data vault of imported cohorts.

How it was evaluated

  • Grounding: a second model checks that every quote appears word for word in the source note. Anything that fails goes to a human.
  • Agreement: reviewers adjudicate a sample, and their verdict is the ground truth.
  • Model changes: an LLM judge compares two runs on the same records, blind, before a model goes to production.
  • Product: scripted test scenarios on the live app before each release.
84.9%records resolved with no reviewer time, lead criterionCompany reported · One study, 114 patients, 2,466 records, Apr 2026
50 / 50reviewed records where the reviewer agreed with the modelCompany reported · Same study

No platform accuracy, precision or recall. 84.9% is the share of records that needed no human check, not an accuracy score. Pairing model and reviewer decisions record by record is the next piece of work.

How it changed

  1. Feb 2026My prototype, as NeuroValidateProve the review loop before spending engineering time
  2. Mar to AprProduction: auth, projects, criteria to run, review, rolesEvery prototype flow but one shipped
  3. JunTrial screening; structured criteria pass automaticallyReviewer time was the expensive step
  4. Jun to JulLocked full runs and an anonymisation flowQuality checks found names in run outputs
  5. JulClear run states and reruns"Pending" looked the same for healthy and crashed jobs
  6. Aug to SepRun log, incremental runs, model comparison, auto prompter, approvals, access controlCost and governance asks from users

Technical choices

  • Keyword retrieval over Elasticsearch with an agent checking keywords first
  • Two pass extraction and grounding, model chosen per criterion from a cost ordered lineup of open and frontier models
  • Go services on AWS, React, MongoDB, queue based workers, per run token and cost tracking

What I learned

  • Grounding beats confidence scores. A word for word quote makes every answer checkable.
  • Reliability, not intelligence, was the top complaint. A clear job status won more trust than a better model.
  • Treat the prototype as the spec, and track what production actually ships.