Sofia Tamini is a Regulatory Affairs Manager with extensive experience in managing regulatory affairs, particularly in the medical devices sector. They have developed expertise in regulatory pathways, CE certification strategies, and compliance documentation, while actively participating in clinical research and medical writing, contributing to over 30 publications in indexed journals. Currently leading the Regulatory Affairs department at PRINEOS, Sofia defines strategies for regulatory compliance and manages interactions with stakeholders, while also serving as a speaker and trainer on medical device regulations and best practices.
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