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.
ISO 13485 audits can intimidate anyone. It sounds rigid and technical, and like it is designed to catch you out. This is why in this article we will walk you through how to prepare for an ISO 13485 audit, without the stress.
The prime directive of medical device manufacturers is the continued safety of patients through safe and effective medical devices. A critical aspect of medical device safety is ensuring regulatory compliance of any medical device destined for the co...
Subscribe to the
Scilife Blog
Life Science and Quality resources and news. All directly to your inbox!
