Arpit Mishra

Arpit Mishra is a seasoned regulatory affairs specialist with over three years of experience in regulatory affairs across various markets, including the EU and ROW. Currently serving as a Senior Regulatory Specialist at Vantive, Arpit has a robust background in managing regulatory submissions for medical devices, particularly 510(k) submissions and EU MDR compliance. Previously, they held positions at Theon Pharmaceuticals Ltd. and Auxein Medical, where they coordinated cross-functional teams and maintained compliance with global regulatory standards. Arpit holds a Bachelor's degree in Pharmacy from Rajasthan University of Health Sciences and is pursuing a Master's in Biomedical Engineering at Shobhit University.