News

Coming soon: MDR-Podden

We are happy to share with you that our Director of regulatory affairs, Sofia Nordgren, soon...

White paper: Medical Device Software – Understanding the impact of the MDR

INTRODUCTION The advancements in technology and digital revolution of the healthcare and medical device industry have created a vast amount of...

Thank you, Nordic Life Science Days!

Thank you Nordic Life Science Days for giving us the opportunity to contribute to your Super...

Nordic Life Science Investment Day – Where Are We & How Did We Get Here?

Nordic Life Science Investment Day: Modernizing the Regulatory Landscape – Where Are We & How Did We Get Here? The 21st...

MedTech compliance made easy – Visit Kickfile’s new webpage!

MedTech compliance made easy - Visit Kickfile's new webpage!  

Reasons to why standardizing is necessary

Devicia are proud to be a part of both the SIS Technical Committée (SIS/TK 340) and the technical committee...

Biocompatibility course – Practical perspective & regulatory aspects

Do you want to develop your basic understanding of biocompatibility related issues? Don’t miss out on this virtual course hosted by...

GoCo Health Innovation City – A powerful step forward

Key profiles from business, health care and the academy collaborate to make GoCo Health Innovation City...