Medha Bharadwaj

Medha Bharadwaj is a Senior Regulatory Affairs Specialist with extensive experience in the medical device industry, currently serving at Intuitive since September 2022 as the primary regulatory lead for new product development in robotic-assisted surgery. Prior to this role, Medha worked at FUJIFILM Sonosite, Inc. from July 2017 to September 2022, providing regulatory guidance for Class II ultrasound systems. Medha's background also includes a position at LivaNova, where responsibilities encompassed regulatory affairs for Class III devices, including the preparation of FDA submissions and research on international requirements. Experience as a Graduate Researcher at the Laboratory for Computational Neurodiagnostics involved developing algorithms for fMRI data analysis. Medha holds a Master of Science in Biomedical/Medical Engineering from Stony Brook University and a Bachelor of Engineering in Medical Electronics Engineering from B. M. S. College of Engineering.