Sathya S

Sathya S is a dedicated Medical Device Regulatory Professional with a background in Biomedical Engineering and over 8 years of experience in the medical device and pharmaceutical industries. Currently serving as a Regulatory Affairs Manager at Philips, Sathya has held various roles where they excelled in regulatory strategy, compliance, and audit management, including successful transitions related to EU MDR and Notified Body changes. Previously, Sathya worked with notable companies such as Novo Nordisk, Biocon, and PERFINT Healthcare, contributing to product development, regulatory submissions, and cross-functional collaboration. Sathya holds a Bachelor’s Degree in Biomedical/Medical Engineering from PSG College of Technology, where they graduated with First Class honors.