EU AI Act Resource Pack
Printable PDF documents for your compliance team: checklist, risk classification, and deadline overview. Enter your email to download instantly.
AI Act Article 50 Disclosure Pack (v1)
A practical checklist and copy/paste disclosure templates you can ship today (plus marking and evidence guidance).
What's inside
- Product/UI checklist for Article 50
- Copy/paste disclosure strings
- Marking/watermarking guidance + logging fields
- Evidence artifacts checklist
EU AI Act Compliance Checklist
A 12-section printable checklist covering every obligation for high-risk AI system providers and deployers.
What's inside
- Role determination (Provider vs Deployer)
- Risk classification walkthrough
- Articles 9-15 requirements checklist
- Conformity assessment and CE marking
- Post-market monitoring duties
AI Act Risk Classification Flowchart
A 7-step decision tree to classify any AI system as Unacceptable, High, Limited, or Minimal risk.
What's inside
- Article 5 prohibited practices check
- Annex III high-risk use case areas
- Article 6(3) exception analysis
- Transparency obligation triggers
- Risk level summary with articles
EU AI Act Enforcement Timeline
Visual timeline from August 2024 through August 2027 showing every enforcement milestone and penalty.
What's inside
- All 4 enforcement milestones with dates
- Specific obligations per milestone
- Penalty overview (€35M / 7% turnover)
- Status indicators (in effect / upcoming)
- Next steps and free assessment link
AI Act × MDR/IVDR Crosswalk
For medical-AI teams: an obligation-by-obligation map of what your MDR/IVDR conformity already covers and what the AI Act adds.
What's inside
- The Art 6(1) high-risk trigger (MDR/IVDR class → outcome)
- MDR and IVDR class tables (notified body → high-risk)
- Article-by-article crosswalk vs ISO 13485/14971
- What Art 43(3) integrates into one procedure
- A printable Have / Partial / Gap status column
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