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.
Standard Operating Procedures (SOPs) are the backbone of quality management systems in the life sciences industry. Whether you're working in pharmaceuticals, medical devices, or biotechnology, SOPs ensure consistency, compliance, and safety in proces...
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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