Market Intelligence
Global Market Access Intelligence
Map regulatory pathways, track market entry signals, and identify cross-border expansion opportunities — powered by global public sources and semantic knowledge graphs.
Markets We Track
Data sources across every major regulatory market
North America
- FDA (USA) — 510(k), PMA, De Novo
- Health Canada — MDALL, device licenses
- USPTO — patent filings and grants
- CMS — reimbursement and coverage
Europe
- EUDAMED — IVDR/MDR certificates
- EU CTIS — clinical trial registry
- EPO — European patent filings
- WHO Prequalification
Asia-Pacific
- NMPA (China) — device registrations
- PMDA (Japan) — premarket approvals
- MFDS (South Korea) — device certifications
- TGA (Australia) — ARTG listings
Latin America
- ANVISA (Brazil) — device registrations
- COFEPRIS (Mexico) — sanitary authorizations
- INVIMA (Colombia) — medical device registry
- ANMAT (Argentina) — device approvals
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Ready to Expand Globally?
Navigate regulatory pathways and market entry requirements with signal intelligence. Track harmonization trends, reimbursement shifts, and competitive landscapes across 24 data sources.