> ## 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.

# Introduction

> Real-time regulatory intelligence for medical devices

# 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.

## What can you do with Qalico?

<CardGroup cols={2}>
  <Card title="Claude Connector" icon="link" href="/claude-connector/overview">
    Connect Qalico to Claude and get regulatory intelligence directly in your conversations.
  </Card>

  <Card title="REST API" icon="code" href="/api-reference/overview">
    Integrate regulatory data into your own products with our REST API.
  </Card>
</CardGroup>

## 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