Tosan Eweka

Tosan Eweka is a seasoned regulatory affairs professional with extensive experience in the medical device sector. Currently serving as a Principal Regulatory Affairs Specialist at Inari Medical since June 2022, Tosan is responsible for regulatory submissions, including 510Ks and Pre-Subs, and reviews clinical data to support these processes. Previously, Tosan held the role of Regulatory Affairs Manager at Quest Medical, Inc., overseeing the compilation and maintenance of EU Technical files and facilitating FDA 510(k) submissions. Tosan's career also includes positions as Regulatory Affairs/Quality Assurance Supervisor at CTL Amedica, Regulatory Affairs Associate at AccelSpine, and Senior Supervisor, Legal at the Securities and Exchange Commission in Nigeria. Tosan holds a Master of Laws (LLM) from The University of Manchester and a Bachelor of Laws (LLB) from the University of Benin.