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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.

  1. Scheduled scanFDA + EU sources
  2. New documentsDe-duplicated
  3. AI summaryWhat changed, who's affected
  4. DashboardSearchable, categorised
  5. 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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