Aesthetic Devices Regulatory Compliance and Safety Standards Course: FDA Guidelines and EU Medical Device Regulations (MDR 2017/745), (ONLIVE EVENT: June 12, 2026)

AI Briefing

• – Aesthetic devices industry professionals will learn about FDA guidelines and EU MDR 2017/745 regulations.
• – Understanding global safety standards and effective marketing strategies will be discussed.
• – Navigating classification complexities and regional regulations will be covered for market entry and credibility.