Regulatory Affairs Consultant
Mari is part of the US Regulatory Affairs team. Mari is an expert in different class devices for the US, EU, Japan and Canada Medical Device Regulations. She has been involved in regulatory compliance projects for several types of non-active devices.
Before joining Qserve, she worked as a Senior RA Specialist at Stryker Neurovascular. Her scope of work included Submissions (510(k), Design Dossier, Technical File, PMDA), global regulatory strategy, post-market change assessment, interaction with regulatory authorities.
Mari has a Bachelor’s degree in Political Science and is currently pursuing a Master’s degree in Regulatory Science at University
of Southern California.
Learn more about our services within Regulatory Affairs