Emma Talvitie

Emma Talvitie is a Regulatory Affairs Expert in the medical devices and in vitro diagnostics field. With a Master of Science in Biotechnology, Emma has a diverse background that includes experience as an R&D Scientist, Technical Writer, Thesis Worker, and Project Specialist. Emma has a strong foundation in laboratory work, project planning, and documentation, making their a valuable asset in the regulatory affairs sector. Emma's previous roles have equipped their with skills in assay verification, validation, and compliance with EU regulations.