Industry starterIndustry-Specific

Healthcare

Regions

Global, US, EU, UK, AU, CA

Source references

6 source references

Control areas

4 mapped control areas

Deployment options

Regulated SaaS, Sovereign region

About this template

A clinician asks a question and pastes the chart to save time. The record number, the insurer and the address travel with it. This starter treats that as the normal case rather than the exception. It masks health detail before the model sees it and keeps the assistant out of diagnosis and prescribing.

This is the general health starter, written for a team that works across more than one country. It assumes clinical content will arrive in prompts, and that the safest handling is early masking. Reach for it when a deployment spans several regions and no single national rule governs the workflow.

Injection screening opens at 0.75, and a prompt that reaches the signal is refused. Redaction runs in health mode and masks record numbers, patient identifiers, insurance membership numbers, phone patterns, health card numbers and street addresses. A second pass masks diagnosis and procedure codes, treatment plans, laboratory results, medication schedules and study identifiers. Both passes mask rather than refuse, so a clinician can keep working.

Clinical language limits work on the output. The assistant cannot state a diagnosis, tell a person what they may have, prescribe or change a dose. Two disclaimers are required, pointing the reader to a provider and away from treating the answer as medical advice. A response has to clear a combined 0.80 with accuracy at 0.90 before it is delivered. Citation checks record grounding at a confidence of 0.85 rather than blocking the response.

Interactions are captured in redacted form for clinical audit. The audit marker only shows that an evaluation ran, so storage and retention stay with your own systems. This starter names no jurisdiction, so choose the United States health starter for protected health information rules, or the European one for special category data. Device classification, clinical validation and lawful basis remain decisions for your clinical and legal owners.

Source frameworks, standards and obligations

WHO Digital Health GuidelinesICD-11 Classification StandardsICH GCP GuidelinesWMA Declaration of HelsinkiISO 13485 (Medical Devices QMS)ISO 14971 (Risk Management)

Control areas mapped by this template

Data privacy
Audit logging
Content moderation
Clinical safety

Deployment options

Regulated SaaS
Sovereign region

Adapt the template in three steps

1

Review the scope

Confirm that the regions, source references, control areas and deployment options fit your use case.

2

Adapt the configuration

Open the template in the Verdictan console. Set its policies, thresholds, routing and review requirements for your environment.

3

Test before deployment

Test each policy outcome. Confirm that allowed, redacted, blocked and reviewed requests behave as expected.