Sathya S

Sathya S is a results-driven Medical Device Regulatory Professional and Biomedical Engineer with a strong background in the medical device and pharmaceuticals industry. With approximately 8 years of experience, Sathya has successfully navigated EUMDR transitions and managed Health Authority and Notified Body audits across various classifications of medical devices. Having held positions in notable organizations such as Philips and Novo Nordisk, Sathya has developed expertise in regulatory strategy, technical documentation, and compliance. Committed to knowledge sharing, Sathya actively supports product development teams and embraces a fitness lifestyle to maintain a healthy work-life balance.