Sanjay Terse is a Regulatory Specialist at Carestream Health, bringing over 20 years of experience in the medical device industry. They have a strong background in regulatory affairs and quality assurance, specializing in Class I–IIb devices, including Software as a Medical Device (SaMD). Sanjay is a certified Lead Auditor for ISO 13485 and ISO 9001, with a Bachelor of Engineering in Chemical Engineering from TKIET. Previously, they served as AVP of Quality Assurance and Regulatory Affairs at Trivitron Healthcare, demonstrating expertise in securing global market approvals and building compliant quality management systems.
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