Navnath is interested in the commercialization of medical technology and for 7 years he has been planning regulatory pathways, regulatory submissions, product development, risk management, product optimization, validations, as well as the establishment, implementation, and planning of quality management systems and facilities.

He previously oversaw APAC Regulatory and Quality compliance at Leica Biosystems. Along with leading the Regulatory Information and Facilitation Center (RIFC) in Venture Center, Pune, Navnath collaborated closely with entrepreneurs and device designers to ensure that the devices quality and regulatory operations were up to par. Navnath has multifaceted working experience managing Quality and Regulatory operations at medical devices startup Axio Biosolutions Pvt Ltd Bangalore and Ahmedabad.

Navnath is Master of Pharmacy with a focus on Quality Assurance Techniques and Regulations from Poona College of Pharmacy in Pune, and Postgraduate Diploma in Entrepreneurship Development and Business Management from EDII, Ahmedabad.

Navnath is a certified Lead Auditor for medical devices Quality Management System and a RAPS Credentialed Regulatory Affairs Professional (RAC-Global) for Medical Devices, IVDs, Pharmaceuticals, Medicinal Products, and Biologics.