Sushmitha Sampath

Sushmitha Sampath is a Senior Regulatory Affairs Specialist at Nevro since August 2022, with extensive experience in regulatory affairs for medical devices. Sushmitha has been a member of the Regulatory Affairs Professionals Society (RAPS) since March 2019 and previously held the position of Senior Regulatory Affairs Specialist at Medtronic from July 2019 to August 2022. Sushmitha's expertise includes developing regulatory strategies for markets in the EU, US, and China, authorship of 510(k) submissions for FDA approval, and consultation on device registration processes. Prior roles include RA & QA Consultant at the University of Southern California, Process Improvement Consultant at LAC + USC Medical Center, and various engineering positions, showcasing a strong background in both regulatory and engineering aspects of medical technology. Sushmitha holds a Master's degree in Bioengineering and Biomedical Engineering from the University of Southern California and a Bachelor's degree in Biomedical/Medical Engineering from SSN College of Engineering.