Health tech quality management and regulatory affairs workshop

Workshop goals

Understanding of commercialization & regulations:
• Teams will learn knowledge on medical device commercialization, quality assurance, and regulatory affairs to navigate and apply these requirements effectively.

Skills for medtech and healthtech innovation:
• Training promotes practical skills to integrate regulatory and quality requirements seamlessly into their development cycles.

Effective regulatory strategy understanding:
• Participants will gain confidence to actively support regulatory strategies, understanding how compliance drives successful market access.

Teams will leave with actionable skills in quality assurance and regulatory matters, ready to apply best practices and drive improvements in compliance.

More information coming soon...

Host: Timo Heikkilä

This is an Aalto internal event and only for our internal community.