Marysa Loustalot

Marysa Loustalot is a highly experienced regulatory affairs professional with a diverse background in medical technology and product development. Currently serving as a Staff Regulatory Affairs Specialist at ZEISS Medical Technology since September 2022, Marysa previously held key roles at Invitae, Zest Dental Solutions, Abbott Diagnostics Business, NuVasive, Hansen Medical, and Abbott Vascular, where responsibilities included managing regulatory operations, developing complex regulatory plans, and ensuring compliance with regulations for various medical devices. With expertise in labeling processes, regulatory submissions, and cross-functional collaboration, Marysa has successfully led multiple projects and audits while streamlining regulatory workflows. Marysa holds a B.S. in Biology from the University of the Pacific, enhancing a robust foundation in the regulatory landscape.