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.
More articles from Nanna Finne
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...
Staying ahead of industry shifts has never been more critical for anyone working in biotech, pharma, or MedTech. The pace of innovation is accelerating, regulatory expectations are tightening, and AI is reshaping everything from discovery to commerci...
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