This free webinar introduces the Advanced Master in Regulatory Affairs for Medical Devices (12th ed.) and the Specialized MDR Course (EU) 2017/745 (9th ed.), two AICQ-SICEV qualified programs built on a solid modular framework.

During the session, we will explore the structure, learning objectives, and key differences between the two programs, helping you choose the path that best aligns with your professional development goals.

An opportunity for direct discussion with industry experts to guide your training investment with clarity and confidence.