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Case study 08 · Regulated industries
RegWatch
Monitors FDA and EU AI Act sources, summarises what changed and why it matters.
- n8n
- JavaScript
- LLMs
- Next.js
The problem
Teams in regulated industries have to track constant FDA and EU AI Act updates across many sources — by reading them manually.
What we built
- Scheduled monitoring of FDA and EU AI Act sources
- Automatic de-duplication and categorisation of new documents
- AI summaries of what changed and who it affects
- A searchable dashboard of regulatory activity with open comment periods
How it flows
From trigger to done, step by step.
- Scheduled scanFDA + EU sources
- New documentsDe-duplicated
- AI summaryWhat changed, who's affected
- DashboardSearchable, categorised
- AlertsDeadlines and comment periods
What changed
- ✓One place to see every relevant regulatory change
- ✓Summaries instead of hours of reading
Try it yourself
Infinityy OS runs the same kind of pipeline, live — with fictional data.
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