News

Biocompatibility Matter 2022

We are proud to announce that our partner company Limulus Bio will be hosting the biocompatibility...

The MDR application date is here – Are you ready?

The MDR application date is here – Are you ready? The EU Medical Device Regulation (MDR) EU 2017/745 applies to MedTech...

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...