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Documentation Index

Fetch the complete documentation index at: https://docs.qalico.com/llms.txt

Use this file to discover all available pages before exploring further.

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Welcome to Qalico

Qalico provides real-time regulatory intelligence for medical device manufacturers. We monitor 4,200+ regulatory sources across 60+ countries and agencies, so you never miss a regulatory update.

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What can you do with Qalico?

Claude Connector

Connect Qalico to Claude and get regulatory intelligence directly in your conversations.

REST API

Integrate regulatory data into your own products with our REST API.

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Data coverage

Qalico continuously monitors regulatory sources including:
  • FDA — Guidances, 21 CFR
  • EU — MDR, IVDR, MDCG guidelines, AI Act, harmonized standards
  • ISO/IEC — Full catalog of medical device standards (ISO 13485, ISO 14971, IEC 62304, etc.)
  • Other agencies — Health Canada, PMDA (Japan), TGA (Australia), ANVISA (Brazil), and more