It is in in everyone’s best interest to produce safe, high-quality medical devices, therefore this industry is heavily regulated. But how do you actually plan your regulatory pathway to ensure compliance for your medical device?
Programme
Learn more about strategic regulatory planning to develop your idea into a compliant medical device by a highly experienced life science professional.
Mats H?gberg
Director Medical Device & IVDR, Senior Consultant, RegSmart Life Science AB
Mats is a senior executive with global experience in the medical technology and life sciences market.
Over the past 30+ years, Mats has worked in several international corporations and started two life science companies.
Mats is Medical Engineer with a MSc in industrial Marketing and commercial law and an MBA from Uppsala University.
SPARK Norway Educational Forum are monthly open meetings organized by UiO:Life Science and SPARK Norway partners.