AIFA

Agenzia Italiana del Farmaco

AIFA 🇮🇹 Italy National Active
Home/ Competent Authorities/ Agenzia Italiana del Farmaco

About

AIFA works alongside the Italian Ministry of Health for medical device regulation in Italy. The Italian Ministry of Health's Directorate General for Medical Devices handles device-specific regulation under EU MDR.

Regulatory Details

Regulatory FrameworkEU MDR 2017/745 (Italian implementation)
Device ClassificationClass I, Class IIa, Class IIb, Class III
Jurisdiction TypeNational
Country🇮🇹 Italy
StatusActive

Contact Information

Country🇮🇹 Italy
AddressVia del Tritone 181, 00187 Rome, Italy
Phone+39-06-5978-41

Official Website

Need Regulatory Guidance?

Learn about device registration requirements for this market.

Get in Touch
Scroll to Top