News

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...

White paper: Brexit and its impact on the Medtech Industry

The medical device industry is significantly impacted by Brexit, primarily due to the change in the legal landscape. Notably, the departure...

A part of the technical committee for laboratory medicine (SIS/TK 331)

As of 2014 Devicia has been a proud member of the Swedish Institute for Standard’s technical committee 340, established to...

Support to SOS Children’s Villages

From all of us at Devicia, we would like to say how much we appreciate and enjoy the collaboration we...

Attend the virtual #Biodata2Digi workshop

Do you want to learn more about the Medical Device Regulation and the evidence generation landscape for digital products? Attend the...