Sample output

See what your output will look like

These are faithful structural previews of what each live tool produces — real section headings, real table shapes, real drafting style. The specific content in your generated document will reflect the jurisdiction, industry, staff size, and risk appetite you provide.

These samples are illustrative — not generated documents and not legal advice. Every generated document includes its own review notes and disclaimers.

AI Policy Generator

Word document (.docx)

A 10-section AI usage policy with regulation citations tailored to your jurisdiction and industry.

AI Usage Policy

[Your Organisation] — Responsible AI Use

Draft — for review by in-house practitioners

Table of Contents

  1. 1. Purpose and Scope
  2. 2. Guiding Principles
  3. 3. Permitted Uses of AI
  4. 4. Prohibited Uses and Restrictions
  5. 5. AI Risk Classification
  6. 6. Roles and Responsibilities
  7. 7. Data Governance for AI
  8. 8. Transparency and Explainability Obligations
  9. 9. Incident Response and Reporting
  10. 10. Policy Review and Governance

Plus front-matter and supplementary sections

  • How to Read and Use This Document
  • AI System Inventory
  • Regulatory Watchlist
  • Supplementary A — Network and Information Systems applicability
  • Supplementary B — Data Handling Rules by AI Tool
  • Supplementary C — DPO Obligations
  • Supplementary D — Software-as-a-Medical-Device pathway (where applicable)
  • Policy Sign-off and Review Schedule

3. Permitted Uses of AI

Staff may use approved generative AI tools (listed in Schedule A — Approved AI Tools) to assist with drafting, summarisation, code generation, and research, subject to the data-handling rules in Section 7. AI-assisted code review under EU AI Act Art. 14 (human oversight) requires a named reviewer to evaluate any output that materially influences a customer-facing decision. AI used in clinical decision support is additionally subject to EU MDR Art. 15 (PRRC) and the additional clauses set out in Supplementary D.

(Sample extract — the live document runs ~30 pages, each section drafted with jurisdiction-specific article references and anti-hallucination guards drawn from the regulatory data layer.)

AI Risk Register

Excel workbook (.xlsx) + Word document (.docx) — same register, two formats

A pre-scored register of AI risks mapped to your sector, with likelihood, impact, mitigations, and owners.

Sheet 1 — Risk Register

AI Risk Register — [Your Organisation]

IDRiskLikelihoodImpactScoreRating
R-001Prompt injection in GitHub Copilot-generated codeHigh (4)Critical (5)20Critical
R-002Cross-border data transfer to OpenAI without valid mechanismHigh (4)Critical (5)20Critical
R-003Microsoft Copilot grounding oversharing via SharePoint / TeamsHigh (4)High (4)16High
R-004ChatGPT training-data opt-out and retention uncertaintyHigh (4)High (4)16High
R-005Microsoft Copilot Data Processing Agreement gapsMedium (3)High (4)12High

(Sample extract — the live 14-column register also includes Category, NIST AI RMF function, Regulatory Reference (with specific articles + anti-hallucination guards), Risk Owner, Control Gaps, Recommended Mitigations, and Review Frequency. Above rows are drawn from a real lawyer-validated UAE / technology generation.)

Employee AI Guidelines

Word document (.docx) + Training Matrix (.xlsx) + Glossary (.xlsx)

Plain-language staff guidelines with golden rules, data-handling rules, and an escalation process — plus two Excel companions auto-downloaded alongside.

Employee AI Guidelines

AI use at [Your Organisation] — what staff need to know

Golden rules

  1. 01

    No PHI in unapproved AI tools

    Never paste patient names, dates of birth, medical record numbers, diagnoses, treatments, or any identifier listed under HIPAA Safe Harbor into ChatGPT, Microsoft Copilot, GitHub Copilot, or any AI tool the organisation has not formally approved with a Business Associate Agreement (BAA).

  2. 02

    Verify before you act on AI output

    AI tools — including the ones we approve — generate plausible-looking content that can contain factual errors, fabricated citations, hallucinated medication dosages, or outdated clinical guidance. Treat AI output as a draft for your review, never as a source of truth for clinical or compliance decisions.

  3. 03

    Escalate AI harm within 24 hours

    If an AI tool produces output that you believe is discriminatory, contains a privacy breach, gives unsafe clinical guidance, or materially misleads a patient or colleague, stop using the tool for that task and report to the named AI Incident Owner via the channels listed in Section 8 within 24 hours.

(Sample extract — the full document contains 8–10 golden rules, a multi-row data-handling guide, a printable wallet card, and an incident-reporting flow.)

AI Vendor Assessment

Excel workbook (.xlsx) + Word executive summary (.docx) + Procurement Checklist (.xlsx)

A 30-question scored assessment across six weighted categories, aligned to ISO/IEC 42001 or NIST AI RMF, with auto-summed totals and Pass / Conditional / Reject thresholds — plus a procurement-readiness checklist companion.

Sheet 1 — Scored Assessment

AI Vendor Assessment — [Your Organisation] / [Vendor]

30 questions across 6 weighted categories — aligned to ISO/IEC 42001 or NIST AI RMF (your choice).

Categories & weights

A. Data Protection20%
B. Transparency15%
C. AI Ethics15%
D. Regulatory Compliance20%
E. Cybersecurity20%
F. Vendor Viability10%

Sample question rows

IDQuestionRegulatory call-out
A-01Does the vendor have a current Data Processing Agreement (DPA) covering all categories of personal data the AI service processes?GDPR Art. 28
A-04Does the vendor disclose all sub-processors and notify the customer of changes at least 30 days before processing begins?GDPR Art. 28(2)
B-02Does the vendor publish model card(s) or system documentation covering training data sources, evaluation methods, and known limitations?EU AI Act Art. 13 (provider→deployer)
D-03Does the vendor maintain a system for incident reporting that meets the 72-hour personal-data-breach notification window?GDPR Art. 33
E-05Does the vendor hold a current SOC 2 Type II or ISO/IEC 27001 attestation, with the report or certificate available on request?ISO/IEC 27001:2022

(Sample extract — the live workbook scores each question 0 / 1 / 2, auto-sums the weighted category totals, and renders a Pass / Conditional / Reject threshold for the overall percentage. The Evidence Request List sits as a dedicated tab inside the same workbook; a one-page Executive Summary .docx and a Procurement Checklist .xlsx download alongside.)

AI Compliance Gap Analyser

Excel workbook (.xlsx) + Word executive summary (.docx)

Per-framework gap analysis (EU AI Act / NIST AI RMF / ISO 42001) driven by your self-assessment intake, with an action plan, heat map, 3-phase timeline, and a live Dashboard with native radar + doughnut charts.

Sheet 1 — EU AI Act Gap Analysis

AI Compliance Gap Analysis — [Your Organisation]

Per-framework gap tables driven by your customer self-assessment intake. EU AI Act / NIST AI RMF / ISO 42001 — your choice.

IDObligationCustomer answerGap
EU.1AI literacy programme for all staff (Art. 4)PartialMedium
EU.4Risk management system for high-risk AI systems (Art. 9)NoHigh
EU.5Data governance + dataset quality controls (Art. 10)PartialMedium
EU.7Human oversight measures (Art. 14)YesNone
EU.10Incident reporting to national supervisory authority (Art. 73)NoHigh

(Sample extract — the live workbook contains per-framework gap sheets (EU AI Act / NIST AI RMF / ISO 42001), an Action Plan with phase-banded priorities, a 10-domain Heat Map, a 3-phase implementation Timeline with jurisdiction-specific deadlines, and a live Dashboard with native radar + doughnut charts that auto-refresh as you mark gaps Done. A one-page Executive Summary .docx pairs with the workbook for board sign-off.)

AI Bias Audit Framework

Excel workbook (.xlsx) + Word executive summary (.docx)

A 9-sheet bias-audit framework: risk classification, 34-item audit checklist, fairness testing protocol, RACI, monitoring + remediation, and a live Dashboard.

Sheet 2 — 34-Item Audit Checklist

AI Bias Audit Framework — [Your Organisation]

IDPhaseItemStatus
A.02ScopingDocumented bias-risk profile for the AI system, signed off by accountable ownerCompliant
B.04TestingDisparate-impact ratio computed across protected attributes (race, gender, age, disability)Action needed
C.03GovernanceBias-incident escalation path documented and exercised at least annuallyCritical gap
D.02Sector-specificHealthcare: clinical-equity test data covers all major demographic subgroupsVerify

(Sample extract — the live 9-sheet workbook covers Risk Classification + 34-Item Audit Checklist + Fairness Testing Protocol + Roles & Responsibilities (RACI) + Permitted & Prohibited + Monitoring & Remediation + Action Plan + Readme + Dashboard. The Executive Summary .docx provides a one-page board sign-off cover with the maturity scorecard and top 5 bias risks.)

AI Incident Response Playbook

Excel workbook (.xlsx) + Word executive summary (.docx)

A 9-sheet incident-response playbook: severity matrix, 6-step response, regulator directory, comms templates, evidence checklist, post-incident review, and a live incident log.

Sheet 1 — Severity Matrix

AI Incident Response Playbook — [Your Organisation]

TierSeverityExample triggerResponse window
P1CriticalPersonal data breach (>1,000 individuals); ICO 72h clock startsImmediate
P2HighRegulator complaint; sustained AI hallucination affecting customer decisions< 4h
P3MediumInternal AI misuse; non-public data quality incident< 24h
P4LowSingle-user AI output anomaly; documented and tracked< 5 days
P5InformationalAI tool deprecation notice; vendor advisoryLogged

(Sample extract — the live 9-sheet workbook covers Severity Matrix + 6-Step Response Process + Regulator Directory + 12 jurisdiction-aware Comms Templates + Evidence Checklist + Post-Incident Review + Live Incident Log + Readme + Dashboard. The Executive Summary .docx pairs with the workbook for board sign-off; the workbook is the operational instrument the AI Champion runs the response from.)

AI Governance Dashboard

Excel workbook (.xlsx) + 7-slide PowerPoint board pack (.pptx) + Word executive summary (.docx)

A board-ready governance programme with org structure, RACI, 90-day roadmap, 12-KPI dashboard, board report, audit calendar, and a live-formula Dashboard with native radar + doughnut charts.

Sheet 4 — KPI Dashboard

AI Governance Dashboard — [Your Organisation]

IDKPIBaselineTargetStatus
K-01AI policy adoption rate64%95%Amber
K-04AI-related incident reports / qtr0<3Green
K-06AI training completion rate32%>90%Red
K-09Vendor DPA coverage (%)78%100%Amber
K-12Audit-readiness score (1–5)2.14.0Red

(Sample extract — the live 10-sheet workbook covers Org Structure + RACI Matrix + 90-Day Roadmap + 12-KPI Dashboard + Board Report + Audit Calendar + AI Tool Register + Intake Answers + Readme + a live-formula Dashboard with native Excel radar + doughnut. A 7-slide PowerPoint board pack (.pptx) and a one-page Executive Summary .docx ship alongside — three artefacts, three jobs, same source of truth.)

AI Data Processing Agreement

Word document (.docx)

A draft Data Processing Agreement covering 12 main clauses + 4 schedules (Particulars / TOMs / Sub-Processors / International Transfer Mechanism) with AI-specific contract terms and a 10-item negotiation checklist.

Data Processing Agreement

AI DPA — [Your Organisation] / [AI Vendor]

Draft — for review by qualified legal counsel before execution

Main Clauses

  1. 1. Definitions and Interpretation
  2. 2. Subject Matter and Duration
  3. 3. Nature and Purpose of Processing
  4. 4. Personal Data Categories and Data Subjects
  5. 5. Obligations of the Processor (incl. AI-specific terms)
  6. 6. Security of Processing (Art. 32 GDPR)
  7. 7. Sub-Processing Authorisation
  8. 8. International Data Transfers
  9. 9. Data Subject Rights Assistance
  10. 10. Personal Data Breach Notification
  11. 11. Audit Rights and Compliance Verification
  12. 12. Termination, Return, and Deletion

Schedules

  • Schedule 1 — Particulars of Processing
  • Schedule 2 — Technical and Organisational Measures
  • Schedule 3 — Approved Sub-Processors
  • Schedule 4 — International Transfer Mechanism

(Sample extract — the live document includes AI-specific contract terms (model card disclosures, training-data warranties, sub-processor change-notice windows, prompt + output-data handling), a 10-item negotiation checklist for procurement, regulator-specific notes (ICO / EDPB / OAIC / PDPC), and qualified-legal-review reminders. Single-format DOCX — no companion XLSX.)

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