<img height="1" width="1" style="display:none;" alt="" src="https://px.ads.linkedin.com/collect/?pid=489233&amp;fmt=gif">
Nanna Finne

Nanna Finne

Senior Regulatory Affairs Specialist, Scilife

Nanna has a proven track record of guiding medical device companies through the complexities of compliance across major markets. With an affinity for clinical evaluations, post-market surveillance, and process optimization, she continues her passion for ensuring quality products reach patients and end users. Not one to miss the smaller details, she encourages continuous improvements in everything she does.

A fundamental part of safeguarding patients in Europe comes from ensuring that medical devices and in vitro diagnostics (IVDs) meet consistent, high regulatory standards. Under the EU Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation...

The EU medical device regulatory framework continues to evolve. As EUDAMED modules roll out and MDR timelines shift, many manufacturers are finding that maintaining compliance now requires far more structure and oversight than it did just a few years...

Subscribe to the

Scilife Blog

Life Science and Quality resources and news. All directly to your inbox!

Scilife Skyrocket microscope | Scilife