The Data Developers
Clinical

EMA European Drug Authorization Intelligence

European Medicines Agency authorized products with therapeutic area classification, orphan designation, biosimilar status, and authorization dates. Exact-match bridge to FDA drug identity for dual-market tracking.

1,500+ products Monthly Updated 2026-09-01

Overview

European Medicines Agency authorized products with therapeutic area classification, orphan designation, biosimilar status, and authorization dates. Exact-match bridge to FDA drug identity for dual-market tracking.

Monitor trial, authorization, sponsor, facility, and funding records as query-ready relational tables.

Normalize sponsors to ROR and parent organizations for competitive intelligence and portfolio views.

Map interventions, conditions, MeSH terms, drugs, and protein mechanisms through controlled identifiers.

Surface compliance, funding, geography, and recruitment signals without custom ETL.

Source authority

European Medicines Agency

Freshness

Last refreshed 2026-09-01

Monthly

Coverage

1,500+ products

2 delivery tables