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?
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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.