Regulatory updateRetina
Faricimab: start with the current EU product information
The EMA Vabysmo record is the authoritative entry point for EU product information, assessment documents and authorised indications.
Regulatory
Drug and device decisions, by country and authority.
2 results
Regulatory updateDevice regulation
EUDAMED: four modules are now mandatory
From 28 May 2026, mandatory use applies to actor registration, UDI/device registration, notified bodies and certificates, and market surveillance.