# DocuTwin Documentation Review Demo

## Buyer Brief
- Product: DocuTwin
- Buyer: Clinical documentation, ambulatory operations, and quality leaders
- Agent: Documentation Agent
- Status: executable-demo
- Executable route: /workflows/docutwin-draft-note-review

## Objective
Demonstrate draft-only documentation support that preserves authorship, source trace, missing context, and review control.

## Synthetic Scenario
A synthetic documentation packet produces a reviewable draft state, source trace, missing-context prompts, and blocked final-signature action.

## Guided Evaluation
- Inspect the draft-only workflow contract.
- Review missing-context prompts and source-trace evidence.
- Inspect the deterministic result and validation state.
- Confirm final note signature and EHR filing remain blocked.

## Inspectable Proof
- [Workflow result](/workflows/results/docutwin-draft-note-review): Draft-only result fixture with source trace and review state.
- [DocuTwin module](/modules/docutwin): Documentation workflow scope and clinician-control boundary.
- [AgentOS evaluation](/evaluation): Interactive synthetic document evaluation with Trust Card output.

## Inspectable Outcomes
- Draft note structure
- Source trace
- Missing-context prompts
- Clinician review checklist

## Success Signals
- Documentation review friction reduced
- Source trace completeness
- Missing context surfaced
- Clinician control retained

## Governance Boundaries
- Licensed clinician review remains required.
- Synthetic encounter packet only.
- Draft output cannot become a final clinical record.

## Production Exclusions
- No final note
- No EHR filing
- No diagnosis insertion
- No autonomous clinical documentation

## Product Boundary
SCRIMED demos and pilot programs are governed synthetic evaluations for enterprise buyers. They do not ingest live PHI, diagnose, treat, submit payer transactions, contact patients, mutate production records, or autonomously execute clinical care.

This brief supports enterprise evaluation and pilot scoping. It is not clinical advice, a production authorization, a certification claim, or evidence of autonomous clinical execution.