Michelle Peterson

Michelle Peterson is a Regulatory Affairs Functional Partner for molecular diagnostics Point of Care devices at Roche, where they develop global regulatory strategies and communicate regulatory changes to stakeholders. With extensive experience in Class III medical devices and Companion Diagnostics, Michelle has previously led Scientific Communications with nine direct reports and established a corporate tool for resource allocation within Regulatory Affairs. They have a strong background in PMA, IDE, 510(k), EU MDR, and IVDR processes, and have worked with major organizations including B. Braun Medical and Edwards Lifesciences. Michelle holds a Bachelor’s Degree in Technical Writing, Biology, and German language from The Kutztown University of PA.