Ashish Salunkhe

Ashish Salunkhe is a Regulatory Affairs Program Specialist at ZOLL Medical Corporation as of January 2024, previously serving as a Regulatory Affairs Consultant at Sterling Medical Devices where responsibilities included addressing documentation gaps for medical devices and preparing 510(k) submissions for the US FDA. Prior experience includes working as an MDR - Regulatory Affairs Specialist at Medtronic, focusing on EU Medical Device Regulation compliance, and as a Regulatory Affairs Intern at China Med Device, conducting market expansion strategies across multiple countries. With an educational background that includes a Master’s degree in Pharmacy Administration and Pharmacy Policy and Regulatory Affairs from Northeastern University and a Bachelor's degree in Pharmacy from Mumbai University, Ashish has also held roles in production coordination and education in the pharmaceutical field.