Selva Subramanian E is a Senior Compliance Specialist in Clinical Evaluations, Quality and Regulatory Affairs at Alcon since 2025. Previously, Selva worked as a Medical Writer and Junior Medical Writer in Regulatory Affairs at Celegence from 2021 to 2024 and served as a Regulatory Analyst at Remidio from 2024 to 2025. Selva specializes in global medical device submissions, SaMD/AI-based diagnostics, and is well-versed in compliance with various regulatory standards, including EU MDR/IVDR and ISO certifications.
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