In this episode, we explore the essentials of medical device registration under Italian law and the EU Medical Device Regulation (MDR 2017/745). We cover everything you need to know about the Italian medical device database, the Repertorio, the CND classification system, and the future role of EUDAMED. 🔑 Keywords & Topics:

• Medical device registration process
• Italian Ministry of Health requirements
• EU MDR compliance
• CND code and Repertorio explained
• EUDAMED implementation timeline
• Regulatory strategy for manufacturers and distributors

👩‍⚕️ Whether you’re a manufacturer, authorized representative, importer, distributor, PRRC or RAQA professional, this episode will help you avoid mistakes and stay compliant with the latest medical device regulations. 👉 Listen now and stay updated on regulatory affairs for medical devices.

#MedicalDevices #RegulatoryAffairs #MDR745 #EUDAMED #MedicalDeviceCompliance #HealthcareRegulation #RAQA #PRRC