Supriya Dalvi

Supriya Dalvi, PhD, holds a Doctorate in Life Sciences from the University of Mumbai and has over 15 years of experience in regulatory functions within the medical device industry, including 11 years focused on compliance and certification. With expertise in various international standards and regulations, Supriya has successfully led the CE certification process for a wide range of medical devices and has experience working with USFDA and global regulatory bodies. Currently, Supriya is a Principal Regulatory Affairs Specialist at Philips, where they focus on X-Ray devices for EU MDR and USFDA 510(k) registration. Supriya also completed a postgraduate program in Business Administration and Management at the Indian Institute of Management, Kozhikode.